Canonical Allele Identifier: CA1619113418

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356843T= , CM000668.2:g.31356843T=	GRCh38
NC_000006.11:g.31324620T= , CM000668.1:g.31324620T=	GRCh37
NC_000006.10:g.31432599T=	NCBI36
NG_023187.1:g.5370A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1661A=
ENST00000481849.6:n.1661A=
ENST00000497377.6:n.1661A=
ENST00000640094.2:c.188A=	ENSP00000491275.2:p.Asp63=
ENST00000696558.1:c.188A=	ENSP00000512716.1:p.Asp63=
ENST00000696559.1:c.188A=	ENSP00000512717.1:p.Asp63=
ENST00000696560.1:c.188A=	ENSP00000512718.1:p.Asp63=
ENST00000696561.1:c.188A=	ENSP00000512719.1:p.Asp63=
ENST00000696562.1:c.188A=	ENSP00000512720.1:p.Asp63=
ENST00000412585.7:c.188A= MANE Select	ENSP00000399168.2:p.Asp63=
ENST00000412585.6:c.188A=	ENSP00000399168.2:p.Asp63=
ENST00000434333.1:c.221A=	ENSP00000405931.1:p.Asp74=
ENST00000474381.1:n.63A=
ENST00000498007.1:n.209A=
ENST00000603274.1:n.197T=
NM_005514.6:c.188A=	NP_005505.2:p.Asp63=
XM_011514556.1:c.221A=	XP_011512858.1:p.Asp74=
XM_011514557.1:c.188A=	XP_011512859.1:p.Asp63=
XR_926175.1:n.198A=
NM_005514.7:c.188A=	NP_005505.2:p.Asp63=
NM_005514.8:c.188A= MANE Select	NP_005505.2:p.Asp63=