Canonical Allele Identifier: CA2677956008

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355948-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355948T>G , CM000668.2:g.31355948T>G	GRCh38
NC_000006.11:g.31323725T>G , CM000668.1:g.31323725T>G	GRCh37
NC_000006.10:g.31431704T>G	NCBI36
NG_023187.1:g.6265A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2311A>C
ENST00000481849.6:n.2092+219A>C
ENST00000497377.6:n.2092+219A>C
ENST00000640094.2:c.619+219A>C	ENSP00000491275.2:n.619+219A>C
ENST00000696558.1:c.620-142A>C	ENSP00000512716.1:n.620-142A>C
ENST00000696559.1:c.619+219A>C	ENSP00000512717.1:n.619+219A>C
ENST00000696560.1:c.619+219A>C	ENSP00000512718.1:n.619+219A>C
ENST00000696561.1:c.619+219A>C	ENSP00000512719.1:n.619+219A>C
ENST00000696562.1:c.619+219A>C	ENSP00000512720.1:n.619+219A>C
ENST00000412585.7:c.619+219A>C MANE Select	ENSP00000399168.2:n.619+219A>C
ENST00000412585.6:c.619+219A>C	ENSP00000399168.2:n.619+219A>C
ENST00000434333.1:c.652+219A>C	ENSP00000405931.1:n.652+219A>C
ENST00000474381.1:n.713A>C
ENST00000498007.1:n.885+219A>C
NM_005514.6:c.619+219A>C	NP_005505.2:n.619+219A>C
XM_011514556.1:c.652+219A>C	XP_011512858.1:n.652+219A>C
XM_011514557.1:c.619+219A>C	XP_011512859.1:n.619+219A>C
XR_926175.1:n.848A>C
NM_005514.7:c.619+219A>C	NP_005505.2:n.619+219A>C
NM_005514.8:c.619+219A>C MANE Select	NP_005505.2:n.619+219A>C