Canonical Allele Identifier: CA3711281

Gene: HLA-B

Linked Data

• dbSNP Id: rs61744514
• ExAC: 6:31322972 G / A
• gnomAD v2: 6-31322972-G-A
• gnomAD v3: 6-31355195-G-A
• gnomAD v4: 6-31355195-G-A
• COSMIC: COSM1077553
• MyVariant Identifiers: chr6:g.31322972G>A (hg19) ; chr6:g.31355195G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355195G>A , CM000668.2:g.31355195G>A	GRCh38
NC_000006.11:g.31322972G>A , CM000668.1:g.31322972G>A	GRCh37
NC_000006.10:g.31430951G>A	NCBI36
NG_023187.1:g.7018C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2971C>T
ENST00000481849.6:n.2490C>T
ENST00000497377.6:n.2397C>T
ENST00000640094.2:c.895+122C>T	ENSP00000491275.2:n.895+122C>T
ENST00000696558.1:c.993C>T	ENSP00000512716.1:n.993C>T
ENST00000696559.1:c.924C>T	ENSP00000512717.1:p.Ile308=
ENST00000696560.1:c.924C>T	ENSP00000512718.1:p.Ile308=
ENST00000696561.1:c.924C>T	ENSP00000512719.1:p.Ile308=
ENST00000696562.1:c.924C>T	ENSP00000512720.1:p.Ile308=
ENST00000412585.7:c.924C>T MANE Select	ENSP00000399168.2:p.Ile308=
ENST00000640094.1:c.88+122C>T	ENSP00000491275.1:n.88+122C>T
ENST00000412585.6:c.924C>T	ENSP00000399168.2:p.Ile308=
ENST00000463574.1:n.515C>T
NM_005514.6:c.924C>T	NP_005505.2:p.Ile308=
XM_011514556.1:c.957C>T	XP_011512858.1:p.Ile319=
XM_011514557.1:c.895+122C>T	XP_011512859.1:n.895+122C>T
XR_926175.1:n.1363C>T
NM_005514.7:c.924C>T	NP_005505.2:p.Ile308=
NM_005514.8:c.924C>T MANE Select	NP_005505.2:p.Ile308=