Canonical Allele Identifier: CA1619118045

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355066G= , CM000668.2:g.31355066G=	GRCh38
NC_000006.11:g.31322843G= , CM000668.1:g.31322843G=	GRCh37
NC_000006.10:g.31430822G=	NCBI36
NG_023187.1:g.7147C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3059+41C=
ENST00000481849.6:n.2619C=
ENST00000497377.6:n.2526C=
ENST00000640094.2:c.895+251C=	ENSP00000491275.2:n.895+251C=
ENST00000696558.1:c.1081+41C=	ENSP00000512716.1:n.1081+41C=
ENST00000696559.1:c.1012+41C=	ENSP00000512717.1:n.1012+41C=
ENST00000696560.1:c.1012+41C=	ENSP00000512718.1:n.1012+41C=
ENST00000696561.1:c.1012+41C=	ENSP00000512719.1:n.1012+41C=
ENST00000696562.1:c.1012+41C=	ENSP00000512720.1:n.1012+41C=
ENST00000412585.7:c.1012+41C= MANE Select	ENSP00000399168.2:n.1012+41C=
ENST00000640094.1:c.88+251C=	ENSP00000491275.1:n.88+251C=
ENST00000412585.6:c.1012+41C=	ENSP00000399168.2:n.1012+41C=
ENST00000497377.5:n.11C=
NM_005514.6:c.1012+41C=	NP_005505.2:n.1012+41C=
XM_011514556.1:c.1045+41C=	XP_011512858.1:n.1045+41C=
XM_011514557.1:c.895+251C=	XP_011512859.1:n.895+251C=
XR_926175.1:n.1451+41C=
NM_005514.7:c.1012+41C=	NP_005505.2:n.1012+41C=
NM_005514.8:c.1012+41C= MANE Select	NP_005505.2:n.1012+41C=