Canonical Allele Identifier: CA1619119903

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356026G= , CM000668.2:g.31356026G=	GRCh38
NC_000006.11:g.31323803G= , CM000668.1:g.31323803G=	GRCh37
NC_000006.10:g.31431782G=	NCBI36
NG_023187.1:g.6187C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2233C=
ENST00000481849.6:n.2092+141C=
ENST00000497377.6:n.2092+141C=
ENST00000640094.2:c.619+141C=	ENSP00000491275.2:n.619+141C=
ENST00000696558.1:c.619+141C=	ENSP00000512716.1:n.619+141C=
ENST00000696559.1:c.619+141C=	ENSP00000512717.1:n.619+141C=
ENST00000696560.1:c.619+141C=	ENSP00000512718.1:n.619+141C=
ENST00000696561.1:c.619+141C=	ENSP00000512719.1:n.619+141C=
ENST00000696562.1:c.619+141C=	ENSP00000512720.1:n.619+141C=
ENST00000412585.7:c.619+141C= MANE Select	ENSP00000399168.2:n.619+141C=
ENST00000412585.6:c.619+141C=	ENSP00000399168.2:n.619+141C=
ENST00000434333.1:c.652+141C=	ENSP00000405931.1:n.652+141C=
ENST00000474381.1:n.635C=
ENST00000498007.1:n.885+141C=
NM_005514.6:c.619+141C=	NP_005505.2:n.619+141C=
XM_011514556.1:c.652+141C=	XP_011512858.1:n.652+141C=
XM_011514557.1:c.619+141C=	XP_011512859.1:n.619+141C=
XR_926175.1:n.770C=
NM_005514.7:c.619+141C=	NP_005505.2:n.619+141C=
NM_005514.8:c.619+141C= MANE Select	NP_005505.2:n.619+141C=