Canonical Allele Identifier: CA449599580

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31354510-C-T
• MyVariant Identifiers: chr6:g.31322287C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354510C>T , CM000668.2:g.31354510C>T	GRCh38
NC_000006.11:g.31322287C>T , CM000668.1:g.31322287C>T	GRCh37
NC_000006.10:g.31430266C>T	NCBI36
NG_023187.1:g.7703G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3109G>A
ENST00000481849.6:n.3069G>A
ENST00000497377.6:n.2976G>A
ENST00000640094.2:c.945G>A	ENSP00000491275.2:p.Gln315=
ENST00000696558.1:c.1131G>A	ENSP00000512716.1:n.1131G>A
ENST00000696559.1:c.1062G>A	ENSP00000512717.1:p.Gln354=
ENST00000696560.1:c.1062G>A	ENSP00000512718.1:p.Gln354=
ENST00000696561.1:c.1062G>A	ENSP00000512719.1:p.Gln354=
ENST00000696562.1:c.1062G>A	ENSP00000512720.1:p.Gln354=
ENST00000412585.7:c.1062G>A MANE Select	ENSP00000399168.2:p.Gln354=
ENST00000640094.1:c.138G>A	ENSP00000491275.1:p.Gln46=
ENST00000412585.6:c.1062G>A	ENSP00000399168.2:p.Gln354=
ENST00000481849.5:n.297G>A
ENST00000497377.5:n.461G>A
NM_005514.6:c.1062G>A	NP_005505.2:p.Gln354=
XM_011514556.1:c.1095G>A	XP_011512858.1:p.Gln365=
XM_011514557.1:c.945G>A	XP_011512859.1:p.Gln315=
XR_926175.1:n.1501G>A
NM_005514.7:c.1062G>A	NP_005505.2:p.Gln354=
NM_005514.8:c.1062G>A MANE Select	NP_005505.2:p.Gln354=