An allele (UK /lil/ or US /lil/), or allel, is one of a number of alternative forms of the same

gene or same genetic locus.[1][2] Sometimes, different alleles can result in different observable
phenotypic traits, such as different pigmentation. However, most genetic variations result in little
or no observable variation.
Most multicellular organisms have two sets of chromosomes; that is, they are diploid. These
chromosomes are referred to as homologous chromosomes. Diploid organisms have one copy of
each gene (and, therefore, one allele) on each chromosome. If both alleles are the same, they
and the organism are homozygous with respect to that gene. If the alleles are different, they and
the organism are heterozygous with respect to that gene.
The word "allele" is a short form of allelomorph ("other form"), which was used in the early days of
genetics to describe variant forms of a gene detected as different phenotypes. It derives from the
Greek prefix , allel, meaning "reciprocal" or "each other", which itself is related to the Greek
adjective (allos; cognate with Latin "alius"), meaning "other"
In many cases, genotypic interactions between the two alleles at a locus can be described as
dominant or recessive, according to which of the two homozygous phenotypes the heterozygote
most resembles. Where the heterozygote is indistinguishable from one of the homozygotes, the
allele involved is said to be dominant to the other, which is said to be recessive to the former.[3]
The degree and pattern of dominance varies among loci. This type of interaction was first formally
described by Gregor Mendel. However, many traits defy this simple categorization and the
phenotypes are modeled by co-dominance and polygenic inheritance.
The term "wild type" allele is sometimes used to describe an allele that is thought to contribute to
the typical phenotypic character as seen in "wild" populations of organisms, such as fruit flies
(Drosophila melanogaster). Such a "wild type" allele was historically regarded as dominant,
common, and normal, in contrast to "mutant" alleles regarded as recessive, rare, and frequently
deleterious. It was formerly thought that most individuals were homozygous for the "wild type"
allele at most gene loci, and that any alternative "mutant" allele was found in homozygous form in
a small minority of "affected" individuals, often as genetic diseases, and more frequently in
heterozygous form in "carriers" for the mutant allele. It is now appreciated that most or all gene
loci are highly polymorphic, with multiple alleles, whose frequencies vary from population to
population, and that a great deal of genetic variation is hidden in the form of alleles that do not
produce obvious phenotypic differences.
Multiple alleles[edit]

Eye color is an inherited trait influenced by more than one gene, including OCA2 and HERC2.
The interaction of multiple genesand the variation in these genes ("alleles") between individuals
help to determine a person's eye color phenotype. Eye color is influenced by pigmentation of
the iris and the frequency-dependence of the light scattering by the turbid medium within the
stroma of the iris.
In the ABO blood group system, a person with Type A blood displays A-antigens and may have a
genotype IAIA or IAi. A person with Type B blood displays B-antigens and may have the genotype
IBIB or IBi. A person with Type AB blood displays both A- and B-antigens and has the genotype
IAIB and a person with Type O blood, displaying neither antigen, has the genotype ii.
A population or species of organisms typically includes multiple alleles at each locus among
various individuals. Allelic variation at a locus is measurable as the number of alleles
(polymorphism) present, or the proportion of heterozygotes in the population.

For example, at the gene locus for the ABO blood type carbohydrate antigens in humans,[4]
classical genetics recognizes three alleles, IA, IB, and i, that determine compatibility of blood
transfusions. Any individual has one of six possible genotypes (IAIA, IAi, IBIB, IBi, IAIB, and ii)
that produce one of four possible phenotypes: "Type A" (produced by IAIA homozygous and IAi
heterozygous genotypes), "Type B" (produced by IBIB homozygous and IBi heterozygous
genotypes), "Type AB" produced by IAIB heterozygous genotype, and "Type O" produced by ii
homozygous genotype. It is now known that each of the A, B, and O alleles is actually a class of
multiple alleles with different DNA sequences that produce proteins with identical properties: more
than 70 alleles are known at the ABO locus.[5] An individual with "Type A" blood may be an AO
heterozygote, an AA homozygote, or an AA heterozygote with two different "A" alleles.
Allele and genotype frequencies[edit]
The frequency of alleles in a diploid population can be used to predict the frequencies of the
corresponding genotypes (see Hardy-Weinberg principle). For a simple model, with two alleles:
p + q=1 \,
p^2 + 2pq + q^2=1 \,
where p is the frequency of one allele and q is the frequency of the alternative allele, which
necessarily sum to unity. Then, p2 is the fraction of the population homozygous for the first allele,
2pq is the fraction of heterozygotes, and q2 is the fraction homozygous for the alternative allele. If
the first allele is dominant to the second then the fraction of the population that will show the
dominant phenotype is p2 + 2pq, and the fraction with the recessive phenotype is q2.
With three alleles:
p + q + r = 1 \, and
p^2 + 2pq + 2pr + q^2 + 2qr + r^2 = 1. \,
In the case of multiple alleles at a diploid locus, the number of possible genotypes (G) with a
number of alleles (a) is given by the expression:
G= \frac{a(a+1)}{2}.
Allelic dominance in genetic disorders[edit]
A number of genetic disorders are caused when an individual inherits two recessive alleles for a
single-gene trait. Recessive genetic disorders include Albinism, Cystic Fibrosis, Galactosemia,
Phenylketonuria (PKU), and Tay-Sachs Disease. Other disorders are also due to recessive
alleles, but because the gene locus is located on the X chromosome, so that males have only one
copy (that is, they are hemizygous), they are more frequent in males than in females. Examples
include red-green color blindness and Fragile X syndrome.
Other disorders, such as Huntington disease, occur when an individual inherits only one dominant
allele.