Canonical Allele Identifier: CA1619112912

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356723_31356724delinsCG , CM000668.2:g.31356723_31356724delinsCG	GRCh38
NC_000006.11:g.31324500_31324501delinsCG , CM000668.1:g.31324500_31324501delinsCG	GRCh37
NC_000006.10:g.31432479_31432480delinsCG	NCBI36
NG_023187.1:g.5489_5490delinsCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1780_1781delinsCG
ENST00000481849.6:n.1780_1781delinsCG
ENST00000497377.6:n.1780_1781delinsCG
ENST00000640094.2:c.307_308delinsCG	ENSP00000491275.2:p.Arg103=
ENST00000696558.1:c.307_308delinsCG	ENSP00000512716.1:p.Arg103=
ENST00000696559.1:c.307_308delinsCG	ENSP00000512717.1:p.Arg103=
ENST00000696560.1:c.307_308delinsCG	ENSP00000512718.1:p.Arg103=
ENST00000696561.1:c.307_308delinsCG	ENSP00000512719.1:p.Arg103=
ENST00000696562.1:c.307_308delinsCG	ENSP00000512720.1:p.Arg103=
ENST00000412585.7:c.307_308delinsCG MANE Select	ENSP00000399168.2:p.Arg103=
ENST00000412585.6:c.307_308delinsCG	ENSP00000399168.2:p.Arg103=
ENST00000434333.1:c.340_341delinsCG	ENSP00000405931.1:p.Arg114=
ENST00000474381.1:n.182_183delinsCG
ENST00000498007.1:n.328_329delinsCG
ENST00000603274.1:n.77_78delinsCG
NM_005514.6:c.307_308delinsCG	NP_005505.2:p.Arg103=
XM_011514556.1:c.340_341delinsCG	XP_011512858.1:p.Arg114=
XM_011514557.1:c.307_308delinsCG	XP_011512859.1:p.Arg103=
XR_926175.1:n.317_318delinsCG
NM_005514.7:c.307_308delinsCG	NP_005505.2:p.Arg103=
NM_005514.8:c.307_308delinsCG MANE Select	NP_005505.2:p.Arg103=