Canonical Allele Identifier: CA2677952928

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354040-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354040G>T , CM000668.2:g.31354040G>T	GRCh38
NC_000006.11:g.31321817G>T , CM000668.1:g.31321817G>T	GRCh37
NC_000006.10:g.31429796G>T	NCBI36
NG_023187.1:g.8173C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3397C>A
ENST00000481849.6:n.3357C>A
ENST00000497377.6:n.3264C>A
ENST00000696558.1:c.1419C>A	ENSP00000512716.1:n.1419C>A
ENST00000696559.1:c.*261C>A	ENSP00000512717.1:n.*261C>A
ENST00000696560.1:c.*261C>A	ENSP00000512718.1:n.*261C>A
ENST00000696561.1:c.*261C>A	ENSP00000512719.1:n.*261C>A
ENST00000696562.1:c.*261C>A	ENSP00000512720.1:n.*261C>A
ENST00000412585.7:c.*261C>A MANE Select	ENSP00000399168.2:n.*261C>A
ENST00000412585.6:c.*261C>A	ENSP00000399168.2:n.*261C>A
ENST00000481849.5:n.585C>A
ENST00000497377.5:n.749C>A
NM_005514.6:c.*261C>A	NP_005505.2:n.*261C>A
XM_011514556.1:c.*261C>A	XP_011512858.1:n.*261C>A
XM_011514557.1:c.*261C>A	XP_011512859.1:n.*261C>A
XR_926175.1:n.1789C>A
NM_005514.7:c.*261C>A	NP_005505.2:n.*261C>A
NM_005514.8:c.*261C>A MANE Select	NP_005505.2:n.*261C>A