Canonical Allele Identifier: CA2677956905
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356431_31356440dup , CM000668.2:g.31356431_31356440dup GRCh38
NC_000006.11:g.31324208_31324217dup , CM000668.1:g.31324208_31324217dup GRCh37
NC_000006.10:g.31432187_31432196dup NCBI36
NG_023187.1:g.5775_5784dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1821_1830dup
ENST00000481849.6:n.1821_1830dup
ENST00000497377.6:n.1821_1830dup
ENST00000640094.2:c.348_357dup ENSP00000491275.2:p.Gln120SerfsTer22
ENST00000696558.1:c.348_357dup ENSP00000512716.1:p.Gln120SerfsTer22
ENST00000696559.1:c.348_357dup ENSP00000512717.1:p.Gln120SerfsTer22
ENST00000696560.1:c.348_357dup ENSP00000512718.1:p.Gln120SerfsTer22
ENST00000696561.1:c.348_357dup ENSP00000512719.1:p.Gln120SerfsTer22
ENST00000696562.1:c.348_357dup ENSP00000512720.1:p.Gln120SerfsTer22
ENST00000412585.7:c.348_357dup MANE Select ENSP00000399168.2:p.Gln120SerfsTer22
ENST00000412585.6:c.348_357dup ENSP00000399168.2:p.Gln120SerfsTer22
ENST00000434333.1:c.381_390dup ENSP00000405931.1:p.Gln131SerfsTer22
ENST00000474381.1:n.223_232dup
ENST00000498007.1:n.614_623dup
NM_005514.6:c.348_357dup NP_005505.2:p.Gln120SerfsTer22
XM_011514556.1:c.381_390dup XP_011512858.1:p.Gln131SerfsTer22
XM_011514557.1:c.348_357dup XP_011512859.1:p.Gln120SerfsTer22
XR_926175.1:n.358_367dup
NM_005514.7:c.348_357dup NP_005505.2:p.Gln120SerfsTer22
NM_005514.8:c.348_357dup MANE Select NP_005505.2:p.Gln120SerfsTer22