Canonical Allele Identifier: CA2677954132

Gene: HLA-B

Linked Data

• dbSNP Id: rs1337747386
• gnomAD v4: 6-31354479-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354479C>A , CM000668.2:g.31354479C>A	GRCh38
NC_000006.11:g.31322256C>A , CM000668.1:g.31322256C>A	GRCh37
NC_000006.10:g.31430235C>A	NCBI36
NG_023187.1:g.7734G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3140G>T
ENST00000481849.6:n.3100G>T
ENST00000497377.6:n.3007G>T
ENST00000696558.1:c.1162G>T	ENSP00000512716.1:n.1162G>T
ENST00000696559.1:c.*4G>T	ENSP00000512717.1:n.*4G>T
ENST00000696560.1:c.*4G>T	ENSP00000512718.1:n.*4G>T
ENST00000696561.1:c.*4G>T	ENSP00000512719.1:n.*4G>T
ENST00000696562.1:c.*4G>T	ENSP00000512720.1:n.*4G>T
ENST00000412585.7:c.*4G>T MANE Select	ENSP00000399168.2:n.*4G>T
ENST00000412585.6:c.*4G>T	ENSP00000399168.2:n.*4G>T
ENST00000481849.5:n.328G>T
ENST00000497377.5:n.492G>T
NM_005514.6:c.*4G>T	NP_005505.2:n.*4G>T
XM_011514556.1:c.*4G>T	XP_011512858.1:n.*4G>T
XM_011514557.1:c.*4G>T	XP_011512859.1:n.*4G>T
XR_926175.1:n.1532G>T
NM_005514.7:c.*4G>T	NP_005505.2:n.*4G>T
NM_005514.8:c.*4G>T MANE Select	NP_005505.2:n.*4G>T