Canonical Allele Identifier: CA1619113281

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356815_31356817delinsCCG , CM000668.2:g.31356815_31356817delinsCCG	GRCh38
NC_000006.11:g.31324592_31324594delinsCCG , CM000668.1:g.31324592_31324594delinsCCG	GRCh37
NC_000006.10:g.31432571_31432573delinsCCG	NCBI36
NG_023187.1:g.5396_5398delinsCGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1687_1689delinsCGG
ENST00000481849.6:n.1687_1689delinsCGG
ENST00000497377.6:n.1687_1689delinsCGG
ENST00000640094.2:c.214_216delinsCGG	ENSP00000491275.2:p.Arg72=
ENST00000696558.1:c.214_216delinsCGG	ENSP00000512716.1:p.Arg72=
ENST00000696559.1:c.214_216delinsCGG	ENSP00000512717.1:p.Arg72=
ENST00000696560.1:c.214_216delinsCGG	ENSP00000512718.1:p.Arg72=
ENST00000696561.1:c.214_216delinsCGG	ENSP00000512719.1:p.Arg72=
ENST00000696562.1:c.214_216delinsCGG	ENSP00000512720.1:p.Arg72=
ENST00000412585.7:c.214_216delinsCGG MANE Select	ENSP00000399168.2:p.Arg72=
ENST00000412585.6:c.214_216delinsCGG	ENSP00000399168.2:p.Arg72=
ENST00000434333.1:c.247_249delinsCGG	ENSP00000405931.1:p.Arg83=
ENST00000474381.1:n.89_91delinsCGG
ENST00000498007.1:n.235_237delinsCGG
ENST00000603274.1:n.169_171delinsCCG
NM_005514.6:c.214_216delinsCGG	NP_005505.2:p.Arg72=
XM_011514556.1:c.247_249delinsCGG	XP_011512858.1:p.Arg83=
XM_011514557.1:c.214_216delinsCGG	XP_011512859.1:p.Arg72=
XR_926175.1:n.224_226delinsCGG
NM_005514.7:c.214_216delinsCGG	NP_005505.2:p.Arg72=
NM_005514.8:c.214_216delinsCGG MANE Select	NP_005505.2:p.Arg72=