Canonical Allele Identifier: CA449599602

Gene: HLA-B

Linked Data

• MyVariant Identifiers: chr6:g.31322429C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354652C>G , CM000668.2:g.31354652C>G	GRCh38
NC_000006.11:g.31322429C>G , CM000668.1:g.31322429C>G	GRCh37
NC_000006.10:g.31430408C>G	NCBI36
NG_023187.1:g.7561G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3073G>C
ENST00000481849.6:n.3033G>C
ENST00000497377.6:n.2940G>C
ENST00000640094.2:c.909G>C	ENSP00000491275.2:p.Gly303=
ENST00000696558.1:c.1095G>C	ENSP00000512716.1:n.1095G>C
ENST00000696559.1:c.1026G>C	ENSP00000512717.1:p.Gly342=
ENST00000696560.1:c.1026G>C	ENSP00000512718.1:p.Gly342=
ENST00000696561.1:c.1026G>C	ENSP00000512719.1:p.Gly342=
ENST00000696562.1:c.1026G>C	ENSP00000512720.1:p.Gly342=
ENST00000412585.7:c.1026G>C MANE Select	ENSP00000399168.2:p.Gly342=
ENST00000640094.1:c.102G>C	ENSP00000491275.1:p.Gly34=
ENST00000412585.6:c.1026G>C	ENSP00000399168.2:p.Gly342=
ENST00000481849.5:n.155G>C
ENST00000497377.5:n.425G>C
NM_005514.6:c.1026G>C	NP_005505.2:p.Gly342=
XM_011514556.1:c.1059G>C	XP_011512858.1:p.Gly353=
XM_011514557.1:c.909G>C	XP_011512859.1:p.Gly303=
XR_926175.1:n.1465G>C
NM_005514.7:c.1026G>C	NP_005505.2:p.Gly342=
NM_005514.8:c.1026G>C MANE Select	NP_005505.2:p.Gly342=