Canonical Allele Identifier: CA1619114271

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357122G= , CM000668.2:g.31357122G=	GRCh38
NC_000006.11:g.31324899G= , CM000668.1:g.31324899G=	GRCh37
NC_000006.10:g.31432878G=	NCBI36
NG_023187.1:g.5091C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1510C=
ENST00000481849.6:n.1510C=
ENST00000497377.6:n.1510C=
ENST00000640094.2:c.37C=	ENSP00000491275.2:p.Leu13=
ENST00000696558.1:c.37C=	ENSP00000512716.1:p.Leu13=
ENST00000696559.1:c.37C=	ENSP00000512717.1:p.Leu13=
ENST00000696560.1:c.37C=	ENSP00000512718.1:p.Leu13=
ENST00000696561.1:c.37C=	ENSP00000512719.1:p.Leu13=
ENST00000696562.1:c.37C=	ENSP00000512720.1:p.Leu13=
ENST00000412585.7:c.37C= MANE Select	ENSP00000399168.2:p.Leu13=
ENST00000412585.6:c.37C=	ENSP00000399168.2:p.Leu13=
ENST00000434333.1:c.-59C=	ENSP00000405931.1:n.-59C=
ENST00000498007.1:n.58C=
ENST00000603274.1:n.476G=
NM_005514.6:c.37C=	NP_005505.2:p.Leu13=
XM_011514557.1:c.37C=	XP_011512859.1:p.Leu13=
XR_926175.1:n.47C=
NM_005514.7:c.37C=	NP_005505.2:p.Leu13=
NM_005514.8:c.37C= MANE Select	NP_005505.2:p.Leu13=