Canonical Allele Identifier: CA3711837

Gene: HLA-B

Linked Data

• dbSNP Id: rs9281379
• ExAC: 6:31324601 C / CG
• gnomAD v2: 6-31324601-C-CG
• gnomAD v3: 6-31356824-C-CG
• gnomAD v4: 6-31356824-C-CG
• COSMIC: COSM298097
• MyVariant Identifiers: chr6:g.31324601_31324602insG (hg19) ; chr6:g.31356824_31356825insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356824_31356825insG , CM000668.2:g.31356824_31356825insG	GRCh38
NC_000006.11:g.31324601_31324602insG , CM000668.1:g.31324601_31324602insG	GRCh37
NC_000006.10:g.31432580_31432581insG	NCBI36
NG_023187.1:g.5388_5389insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1679_1680insC
ENST00000481849.6:n.1679_1680insC
ENST00000497377.6:n.1679_1680insC
ENST00000640094.2:c.206_207insC	ENSP00000491275.2:p.Glu69AspfsTer30
ENST00000696558.1:c.206_207insC	ENSP00000512716.1:p.Glu69AspfsTer30
ENST00000696559.1:c.206_207insC	ENSP00000512717.1:p.Glu69AspfsTer30
ENST00000696560.1:c.206_207insC	ENSP00000512718.1:p.Glu69AspfsTer30
ENST00000696561.1:c.206_207insC	ENSP00000512719.1:p.Glu69AspfsTer30
ENST00000696562.1:c.206_207insC	ENSP00000512720.1:p.Glu69AspfsTer30
ENST00000412585.7:c.206_207insC MANE Select	ENSP00000399168.2:p.Glu69AspfsTer30
ENST00000412585.6:c.206_207insC	ENSP00000399168.2:p.Glu69AspfsTer30
ENST00000434333.1:c.239_240insC	ENSP00000405931.1:p.Glu80AspfsTer30
ENST00000474381.1:n.81_82insC
ENST00000498007.1:n.227_228insC
ENST00000603274.1:n.178_179insG
NM_005514.6:c.206_207insC	NP_005505.2:p.Glu69AspfsTer30
XM_011514556.1:c.239_240insC	XP_011512858.1:p.Glu80AspfsTer30
XM_011514557.1:c.206_207insC	XP_011512859.1:p.Glu69AspfsTer30
XR_926175.1:n.216_217insC
NM_005514.7:c.206_207insC	NP_005505.2:p.Glu69AspfsTer30
NM_005514.8:c.206_207insC MANE Select	NP_005505.2:p.Glu69AspfsTer30