Canonical Allele Identifier: CA363307932

Gene: HLA-B

Linked Data

• dbSNP Id: rs1430794794
• gnomAD v3: 6-31354508-C-A
• gnomAD v4: 6-31354508-C-A
• COSMIC: COSM5710034
• MyVariant Identifiers: chr6:g.31322285C>A (hg19) ; chr6:g.31354508C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354508C>A , CM000668.2:g.31354508C>A	GRCh38
NC_000006.11:g.31322285C>A , CM000668.1:g.31322285C>A	GRCh37
NC_000006.10:g.31430264C>A	NCBI36
NG_023187.1:g.7705G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3111G>T
ENST00000481849.6:n.3071G>T
ENST00000497377.6:n.2978G>T
ENST00000640094.2:c.947G>T	ENSP00000491275.2:p.Gly316Val
ENST00000696558.1:c.1133G>T	ENSP00000512716.1:n.1133G>T
ENST00000696559.1:c.1064G>T	ENSP00000512717.1:p.Gly355Val
ENST00000696560.1:c.1064G>T	ENSP00000512718.1:p.Gly355Val
ENST00000696561.1:c.1064G>T	ENSP00000512719.1:p.Gly355Val
ENST00000696562.1:c.1064G>T	ENSP00000512720.1:p.Gly355Val
ENST00000412585.7:c.1064G>T MANE Select	ENSP00000399168.2:p.Gly355Val
ENST00000640094.1:c.140G>T	ENSP00000491275.1:p.Gly47Val
ENST00000412585.6:c.1064G>T	ENSP00000399168.2:p.Gly355Val
ENST00000481849.5:n.299G>T
ENST00000497377.5:n.463G>T
NM_005514.6:c.1064G>T	NP_005505.2:p.Gly355Val
XM_011514556.1:c.1097G>T	XP_011512858.1:p.Gly366Val
XM_011514557.1:c.947G>T	XP_011512859.1:p.Gly316Val
XR_926175.1:n.1503G>T
NM_005514.7:c.1064G>T	NP_005505.2:p.Gly355Val
NM_005514.8:c.1064G>T MANE Select	NP_005505.2:p.Gly355Val