Canonical Allele Identifier: CA917712256

Gene: HLA-B

Linked Data

• dbSNP Id: rs796093434

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356226_31356227delinsAG , CM000668.2:g.31356226_31356227delinsAG	GRCh38
NC_000006.11:g.31324003_31324004delinsAG , CM000668.1:g.31324003_31324004delinsAG	GRCh37
NC_000006.10:g.31431982_31431983delinsAG	NCBI36
NG_023187.1:g.5986_5987delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2032_2033delinsCT
ENST00000481849.6:n.2032_2033delinsCT
ENST00000497377.6:n.2032_2033delinsCT
ENST00000640094.2:c.559_560delinsCT	ENSP00000491275.2:p.Glu187Leu
ENST00000696558.1:c.559_560delinsCT	ENSP00000512716.1:p.Glu187Leu
ENST00000696559.1:c.559_560delinsCT	ENSP00000512717.1:p.Glu187Leu
ENST00000696560.1:c.559_560delinsCT	ENSP00000512718.1:p.Glu187Leu
ENST00000696561.1:c.559_560delinsCT	ENSP00000512719.1:p.Glu187Leu
ENST00000696562.1:c.559_560delinsCT	ENSP00000512720.1:p.Glu187Leu
ENST00000412585.7:c.559_560delinsCT MANE Select	ENSP00000399168.2:p.Glu187Leu
ENST00000412585.6:c.559_560delinsCT	ENSP00000399168.2:p.Glu187Leu
ENST00000434333.1:c.592_593delinsCT	ENSP00000405931.1:p.Glu198Leu
ENST00000474381.1:n.434_435delinsCT
ENST00000498007.1:n.825_826delinsCT
NM_005514.6:c.559_560delinsCT	NP_005505.2:p.Glu187Leu
XM_011514556.1:c.592_593delinsCT	XP_011512858.1:p.Glu198Leu
XM_011514557.1:c.559_560delinsCT	XP_011512859.1:p.Glu187Leu
XR_926175.1:n.569_570delinsCT
NM_005514.7:c.559_560delinsCT	NP_005505.2:p.Glu187Leu
NM_005514.8:c.559_560delinsCT MANE Select	NP_005505.2:p.Glu187Leu