Canonical Allele Identifier: CA1619119645

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355899A= , CM000668.2:g.31355899A=	GRCh38
NC_000006.11:g.31323676A= , CM000668.1:g.31323676A=	GRCh37
NC_000006.10:g.31431655A=	NCBI36
NG_023187.1:g.6314T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2360T=
ENST00000481849.6:n.2092+268T=
ENST00000497377.6:n.2092+268T=
ENST00000640094.2:c.619+268T=	ENSP00000491275.2:n.619+268T=
ENST00000696558.1:c.620-93T=	ENSP00000512716.1:n.620-93T=
ENST00000696559.1:c.619+268T=	ENSP00000512717.1:n.619+268T=
ENST00000696560.1:c.619+268T=	ENSP00000512718.1:n.619+268T=
ENST00000696561.1:c.619+268T=	ENSP00000512719.1:n.619+268T=
ENST00000696562.1:c.619+268T=	ENSP00000512720.1:n.619+268T=
ENST00000412585.7:c.619+268T= MANE Select	ENSP00000399168.2:n.619+268T=
ENST00000412585.6:c.619+268T=	ENSP00000399168.2:n.619+268T=
ENST00000434333.1:c.652+268T=	ENSP00000405931.1:n.652+268T=
ENST00000474381.1:n.762T=
ENST00000498007.1:n.885+268T=
NM_005514.6:c.619+268T=	NP_005505.2:n.619+268T=
XM_011514556.1:c.652+268T=	XP_011512858.1:n.652+268T=
XM_011514557.1:c.619+268T=	XP_011512859.1:n.619+268T=
XR_926175.1:n.897T=
NM_005514.7:c.619+268T=	NP_005505.2:n.619+268T=
NM_005514.8:c.619+268T= MANE Select	NP_005505.2:n.619+268T=