Canonical Allele Identifier: CA1619117503

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354634C= , CM000668.2:g.31354634C=	GRCh38
NC_000006.11:g.31322411C= , CM000668.1:g.31322411C=	GRCh37
NC_000006.10:g.31430390C=	NCBI36
NG_023187.1:g.7579G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3091G=
ENST00000481849.6:n.3051G=
ENST00000497377.6:n.2958G=
ENST00000640094.2:c.927G=	ENSP00000491275.2:p.Ala309=
ENST00000696558.1:c.1113G=	ENSP00000512716.1:n.1113G=
ENST00000696559.1:c.1044G=	ENSP00000512717.1:p.Ala348=
ENST00000696560.1:c.1044G=	ENSP00000512718.1:p.Ala348=
ENST00000696561.1:c.1044G=	ENSP00000512719.1:p.Ala348=
ENST00000696562.1:c.1044G=	ENSP00000512720.1:p.Ala348=
ENST00000412585.7:c.1044G= MANE Select	ENSP00000399168.2:p.Ala348=
ENST00000640094.1:c.120G=	ENSP00000491275.1:p.Ala40=
ENST00000412585.6:c.1044G=	ENSP00000399168.2:p.Ala348=
ENST00000481849.5:n.173G=
ENST00000497377.5:n.443G=
NM_005514.6:c.1044G=	NP_005505.2:p.Ala348=
XM_011514556.1:c.1077G=	XP_011512858.1:p.Ala359=
XM_011514557.1:c.927G=	XP_011512859.1:p.Ala309=
XR_926175.1:n.1483G=
NM_005514.7:c.1044G=	NP_005505.2:p.Ala348=
NM_005514.8:c.1044G= MANE Select	NP_005505.2:p.Ala348=