Canonical Allele Identifier: CA2677952722

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31353912-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31353912C>G , CM000668.2:g.31353912C>G	GRCh38
NC_000006.11:g.31321689C>G , CM000668.1:g.31321689C>G	GRCh37
NC_000006.10:g.31429668C>G	NCBI36
NG_023187.1:g.8301G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3525G>C
ENST00000481849.6:n.3485G>C
ENST00000497377.6:n.3392G>C
ENST00000696558.1:c.1547G>C	ENSP00000512716.1:n.1547G>C
ENST00000696559.1:c.*389G>C	ENSP00000512717.1:n.*389G>C
ENST00000696560.1:c.*389G>C	ENSP00000512718.1:n.*389G>C
ENST00000696561.1:c.*389G>C	ENSP00000512719.1:n.*389G>C
ENST00000696562.1:c.*389G>C	ENSP00000512720.1:n.*389G>C
ENST00000412585.7:c.*389G>C MANE Select	ENSP00000399168.2:n.*389G>C
ENST00000412585.6:c.*389G>C	ENSP00000399168.2:n.*389G>C
ENST00000481849.5:n.713G>C
ENST00000497377.5:n.877G>C
NM_005514.6:c.*389G>C	NP_005505.2:n.*389G>C
XM_011514556.1:c.*389G>C	XP_011512858.1:n.*389G>C
XM_011514557.1:c.*389G>C	XP_011512859.1:n.*389G>C
XR_926175.1:n.1917G>C
NM_005514.7:c.*389G>C	NP_005505.2:n.*389G>C
NM_005514.8:c.*389G>C MANE Select	NP_005505.2:n.*389G>C