Canonical Allele Identifier: CA2677953240

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354228-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354228C>G , CM000668.2:g.31354228C>G	GRCh38
NC_000006.11:g.31322005C>G , CM000668.1:g.31322005C>G	GRCh37
NC_000006.10:g.31429984C>G	NCBI36
NG_023187.1:g.7985G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3209G>C
ENST00000481849.6:n.3169G>C
ENST00000497377.6:n.3076G>C
ENST00000696558.1:c.1231G>C	ENSP00000512716.1:n.1231G>C
ENST00000696559.1:c.*73G>C	ENSP00000512717.1:n.*73G>C
ENST00000696560.1:c.*73G>C	ENSP00000512718.1:n.*73G>C
ENST00000696561.1:c.*73G>C	ENSP00000512719.1:n.*73G>C
ENST00000696562.1:c.*73G>C	ENSP00000512720.1:n.*73G>C
ENST00000412585.7:c.*73G>C MANE Select	ENSP00000399168.2:n.*73G>C
ENST00000412585.6:c.*73G>C	ENSP00000399168.2:n.*73G>C
ENST00000481849.5:n.397G>C
ENST00000497377.5:n.561G>C
NM_005514.6:c.*73G>C	NP_005505.2:n.*73G>C
XM_011514556.1:c.*73G>C	XP_011512858.1:n.*73G>C
XM_011514557.1:c.*73G>C	XP_011512859.1:n.*73G>C
XR_926175.1:n.1601G>C
NM_005514.7:c.*73G>C	NP_005505.2:n.*73G>C
NM_005514.8:c.*73G>C MANE Select	NP_005505.2:n.*73G>C