Canonical Allele Identifier: CA566689123
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs773843833
gnomAD v2: 6-31324416-C-A
gnomAD v4: 6-31356639-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356639C>A , CM000668.2:g.31356639C>A GRCh38
NC_000006.11:g.31324416C>A , CM000668.1:g.31324416C>A GRCh37
NC_000006.10:g.31432395C>A NCBI36
NG_023187.1:g.5574G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.1816+49G>T
ENST00000481849.6:n.1816+49G>T
ENST00000497377.6:n.1816+49G>T
ENST00000640094.2:c.343+49G>T ENSP00000491275.2:n.343+49G>T
ENST00000696558.1:c.343+49G>T ENSP00000512716.1:n.343+49G>T
ENST00000696559.1:c.343+49G>T ENSP00000512717.1:n.343+49G>T
ENST00000696560.1:c.343+49G>T ENSP00000512718.1:n.343+49G>T
ENST00000696561.1:c.343+49G>T ENSP00000512719.1:n.343+49G>T
ENST00000696562.1:c.343+49G>T ENSP00000512720.1:n.343+49G>T
ENST00000412585.7:c.343+49G>T MANE Select ENSP00000399168.2:n.343+49G>T
ENST00000412585.6:c.343+49G>T ENSP00000399168.2:n.343+49G>T
ENST00000434333.1:c.376+49G>T ENSP00000405931.1:n.376+49G>T
ENST00000474381.1:n.218+49G>T
ENST00000498007.1:n.413G>T
NM_005514.6:c.343+49G>T NP_005505.2:n.343+49G>T
XM_011514556.1:c.376+49G>T XP_011512858.1:n.376+49G>T
XM_011514557.1:c.343+49G>T XP_011512859.1:n.343+49G>T
XR_926175.1:n.353+49G>T
NM_005514.7:c.343+49G>T NP_005505.2:n.343+49G>T
NM_005514.8:c.343+49G>T MANE Select NP_005505.2:n.343+49G>T