Canonical Allele Identifier: CA1619118262

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355156C= , CM000668.2:g.31355156C=	GRCh38
NC_000006.11:g.31322933C= , CM000668.1:g.31322933C=	GRCh37
NC_000006.10:g.31430912C=	NCBI36
NG_023187.1:g.7057G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3010G=
ENST00000481849.6:n.2529G=
ENST00000497377.6:n.2436G=
ENST00000640094.2:c.895+161G=	ENSP00000491275.2:n.895+161G=
ENST00000696558.1:c.1032G=	ENSP00000512716.1:n.1032G=
ENST00000696559.1:c.963G=	ENSP00000512717.1:p.Val321=
ENST00000696560.1:c.963G=	ENSP00000512718.1:p.Val321=
ENST00000696561.1:c.963G=	ENSP00000512719.1:p.Val321=
ENST00000696562.1:c.963G=	ENSP00000512720.1:p.Val321=
ENST00000412585.7:c.963G= MANE Select	ENSP00000399168.2:p.Val321=
ENST00000640094.1:c.88+161G=	ENSP00000491275.1:n.88+161G=
ENST00000412585.6:c.963G=	ENSP00000399168.2:p.Val321=
ENST00000463574.1:n.554G=
NM_005514.6:c.963G=	NP_005505.2:p.Val321=
XM_011514556.1:c.996G=	XP_011512858.1:p.Val332=
XM_011514557.1:c.895+161G=	XP_011512859.1:n.895+161G=
XR_926175.1:n.1402G=
NM_005514.7:c.963G=	NP_005505.2:p.Val321=
NM_005514.8:c.963G= MANE Select	NP_005505.2:p.Val321=