Canonical Allele Identifier: CA1619114327

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357139_31357140delinsCG , CM000668.2:g.31357139_31357140delinsCG	GRCh38
NC_000006.11:g.31324916_31324917delinsCG , CM000668.1:g.31324916_31324917delinsCG	GRCh37
NC_000006.10:g.31432895_31432896delinsCG	NCBI36
NG_023187.1:g.5073_5074delinsCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1492_1493delinsCG
ENST00000481849.6:n.1492_1493delinsCG
ENST00000497377.6:n.1492_1493delinsCG
ENST00000640094.2:c.19_20delinsCG	ENSP00000491275.2:p.Arg7=
ENST00000696558.1:c.19_20delinsCG	ENSP00000512716.1:p.Arg7=
ENST00000696559.1:c.19_20delinsCG	ENSP00000512717.1:p.Arg7=
ENST00000696560.1:c.19_20delinsCG	ENSP00000512718.1:p.Arg7=
ENST00000696561.1:c.19_20delinsCG	ENSP00000512719.1:p.Arg7=
ENST00000696562.1:c.19_20delinsCG	ENSP00000512720.1:p.Arg7=
ENST00000412585.7:c.19_20delinsCG MANE Select	ENSP00000399168.2:p.Arg7=
ENST00000412585.6:c.19_20delinsCG	ENSP00000399168.2:p.Arg7=
ENST00000434333.1:c.-77_-76delinsCG	ENSP00000405931.1:n.-77_-76delinsCG
ENST00000498007.1:n.40_41delinsCG
ENST00000603274.1:n.493_494delinsCG
NM_005514.6:c.19_20delinsCG	NP_005505.2:p.Arg7=
XM_011514557.1:c.19_20delinsCG	XP_011512859.1:p.Arg7=
XR_926175.1:n.29_30delinsCG
NM_005514.7:c.19_20delinsCG	NP_005505.2:p.Arg7=
NM_005514.8:c.19_20delinsCG MANE Select	NP_005505.2:p.Arg7=