Canonical Allele Identifier: CA1619118696

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355341G= , CM000668.2:g.31355341G=	GRCh38
NC_000006.11:g.31323118G= , CM000668.1:g.31323118G=	GRCh37
NC_000006.10:g.31431097G=	NCBI36
NG_023187.1:g.6872C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2918C=
ENST00000481849.6:n.2344C=
ENST00000497377.6:n.2344C=
ENST00000640094.2:c.871C=	ENSP00000491275.2:p.Pro291=
ENST00000696558.1:c.940C=	ENSP00000512716.1:n.940C=
ENST00000696559.1:c.871C=	ENSP00000512717.1:p.Pro291=
ENST00000696560.1:c.871C=	ENSP00000512718.1:p.Pro291=
ENST00000696561.1:c.871C=	ENSP00000512719.1:p.Pro291=
ENST00000696562.1:c.871C=	ENSP00000512720.1:p.Pro291=
ENST00000412585.7:c.871C= MANE Select	ENSP00000399168.2:p.Pro291=
ENST00000640094.1:c.64C=	ENSP00000491275.1:p.Pro22=
ENST00000412585.6:c.871C=	ENSP00000399168.2:p.Pro291=
ENST00000463574.1:n.462C=
NM_005514.6:c.871C=	NP_005505.2:p.Pro291=
XM_011514556.1:c.904C=	XP_011512858.1:p.Pro302=
XM_011514557.1:c.871C=	XP_011512859.1:p.Pro291=
XR_926175.1:n.1310C=
NM_005514.7:c.871C=	NP_005505.2:p.Pro291=
NM_005514.8:c.871C= MANE Select	NP_005505.2:p.Pro291=