Canonical Allele Identifier: CA2677957752

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356821-C-CTCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356824_31356825insATCC , CM000668.2:g.31356824_31356825insATCC	GRCh38
NC_000006.11:g.31324601_31324602insATCC , CM000668.1:g.31324601_31324602insATCC	GRCh37
NC_000006.10:g.31432580_31432581insATCC	NCBI36
NG_023187.1:g.5391_5392insTGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1682_1683insTGGA
ENST00000481849.6:n.1682_1683insTGGA
ENST00000497377.6:n.1682_1683insTGGA
ENST00000640094.2:c.209_210insTGGA	ENSP00000491275.2:p.Glu70AspfsTer30
ENST00000696558.1:c.209_210insTGGA	ENSP00000512716.1:p.Glu70AspfsTer30
ENST00000696559.1:c.209_210insTGGA	ENSP00000512717.1:p.Glu70AspfsTer30
ENST00000696560.1:c.209_210insTGGA	ENSP00000512718.1:p.Glu70AspfsTer30
ENST00000696561.1:c.209_210insTGGA	ENSP00000512719.1:p.Glu70AspfsTer30
ENST00000696562.1:c.209_210insTGGA	ENSP00000512720.1:p.Glu70AspfsTer30
ENST00000412585.7:c.209_210insTGGA MANE Select	ENSP00000399168.2:p.Glu70AspfsTer30
ENST00000412585.6:c.209_210insTGGA	ENSP00000399168.2:p.Glu70AspfsTer30
ENST00000434333.1:c.242_243insTGGA	ENSP00000405931.1:p.Glu81AspfsTer30
ENST00000474381.1:n.84_85insTGGA
ENST00000498007.1:n.230_231insTGGA
ENST00000603274.1:n.178_179insATCC
NM_005514.6:c.209_210insTGGA	NP_005505.2:p.Glu70AspfsTer30
XM_011514556.1:c.242_243insTGGA	XP_011512858.1:p.Glu81AspfsTer30
XM_011514557.1:c.209_210insTGGA	XP_011512859.1:p.Glu70AspfsTer30
XR_926175.1:n.219_220insTGGA
NM_005514.7:c.209_210insTGGA	NP_005505.2:p.Glu70AspfsTer30
NM_005514.8:c.209_210insTGGA MANE Select	NP_005505.2:p.Glu70AspfsTer30