Canonical Allele Identifier: CA1619111473

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356249_31356250delinsCT , CM000668.2:g.31356249_31356250delinsCT	GRCh38
NC_000006.11:g.31324026_31324027delinsCT , CM000668.1:g.31324026_31324027delinsCT	GRCh37
NC_000006.10:g.31432005_31432006delinsCT	NCBI36
NG_023187.1:g.5963_5964delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2009_2010delinsAG
ENST00000481849.6:n.2009_2010delinsAG
ENST00000497377.6:n.2009_2010delinsAG
ENST00000640094.2:c.536_537delinsAG	ENSP00000491275.2:p.Gln179=
ENST00000696558.1:c.536_537delinsAG	ENSP00000512716.1:p.Gln179=
ENST00000696559.1:c.536_537delinsAG	ENSP00000512717.1:p.Gln179=
ENST00000696560.1:c.536_537delinsAG	ENSP00000512718.1:p.Gln179=
ENST00000696561.1:c.536_537delinsAG	ENSP00000512719.1:p.Gln179=
ENST00000696562.1:c.536_537delinsAG	ENSP00000512720.1:p.Gln179=
ENST00000412585.7:c.536_537delinsAG MANE Select	ENSP00000399168.2:p.Gln179=
ENST00000412585.6:c.536_537delinsAG	ENSP00000399168.2:p.Gln179=
ENST00000434333.1:c.569_570delinsAG	ENSP00000405931.1:p.Gln190=
ENST00000474381.1:n.411_412delinsAG
ENST00000498007.1:n.802_803delinsAG
NM_005514.6:c.536_537delinsAG	NP_005505.2:p.Gln179=
XM_011514556.1:c.569_570delinsAG	XP_011512858.1:p.Gln190=
XM_011514557.1:c.536_537delinsAG	XP_011512859.1:p.Gln179=
XR_926175.1:n.546_547delinsAG
NM_005514.7:c.536_537delinsAG	NP_005505.2:p.Gln179=
NM_005514.8:c.536_537delinsAG MANE Select	NP_005505.2:p.Gln179=