Canonical Allele Identifier: CA363310133

Gene: HLA-B

Linked Data

• MyVariant Identifiers: chr6:g.31323123C>A (hg19) ; chr6:g.31355346C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355346C>A , CM000668.2:g.31355346C>A	GRCh38
NC_000006.11:g.31323123C>A , CM000668.1:g.31323123C>A	GRCh37
NC_000006.10:g.31431102C>A	NCBI36
NG_023187.1:g.6867G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2913G>T
ENST00000481849.6:n.2339G>T
ENST00000497377.6:n.2339G>T
ENST00000640094.2:c.866G>T	ENSP00000491275.2:p.Gly289Val
ENST00000696558.1:c.935G>T	ENSP00000512716.1:n.935G>T
ENST00000696559.1:c.866G>T	ENSP00000512717.1:p.Gly289Val
ENST00000696560.1:c.866G>T	ENSP00000512718.1:p.Gly289Val
ENST00000696561.1:c.866G>T	ENSP00000512719.1:p.Gly289Val
ENST00000696562.1:c.866G>T	ENSP00000512720.1:p.Gly289Val
ENST00000412585.7:c.866G>T MANE Select	ENSP00000399168.2:p.Gly289Val
ENST00000640094.1:c.59G>T	ENSP00000491275.1:p.Gly20Val
ENST00000412585.6:c.866G>T	ENSP00000399168.2:p.Gly289Val
ENST00000463574.1:n.457G>T
NM_005514.6:c.866G>T	NP_005505.2:p.Gly289Val
XM_011514556.1:c.899G>T	XP_011512858.1:p.Gly300Val
XM_011514557.1:c.866G>T	XP_011512859.1:p.Gly289Val
XR_926175.1:n.1305G>T
NM_005514.7:c.866G>T	NP_005505.2:p.Gly289Val
NM_005514.8:c.866G>T MANE Select	NP_005505.2:p.Gly289Val