Canonical Allele Identifier: CA449790699

Gene: HLA-B

Linked Data

• dbSNP Id: rs1478381844
• gnomAD v2: 6-31324002-C-CG
• gnomAD v3: 6-31356225-C-CG
• gnomAD v4: 6-31356225-C-CG
• MyVariant Identifiers: chr6:g.31324002_31324003insG (hg19) ; chr6:g.31356225_31356226insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356225_31356226insG , CM000668.2:g.31356225_31356226insG	GRCh38
NC_000006.11:g.31324002_31324003insG , CM000668.1:g.31324002_31324003insG	GRCh37
NC_000006.10:g.31431981_31431982insG	NCBI36
NG_023187.1:g.5987_5988insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2033_2034insC
ENST00000481849.6:n.2033_2034insC
ENST00000497377.6:n.2033_2034insC
ENST00000640094.2:c.560_561insC	ENSP00000491275.2:p.Glu187AspfsTer21
ENST00000696558.1:c.560_561insC	ENSP00000512716.1:p.Glu187AspfsTer21
ENST00000696559.1:c.560_561insC	ENSP00000512717.1:p.Glu187AspfsTer21
ENST00000696560.1:c.560_561insC	ENSP00000512718.1:p.Glu187AspfsTer21
ENST00000696561.1:c.560_561insC	ENSP00000512719.1:p.Glu187AspfsTer21
ENST00000696562.1:c.560_561insC	ENSP00000512720.1:p.Glu187AspfsTer21
ENST00000412585.7:c.560_561insC MANE Select	ENSP00000399168.2:p.Glu187AspfsTer21
ENST00000412585.6:c.560_561insC	ENSP00000399168.2:p.Glu187AspfsTer21
ENST00000434333.1:c.593_594insC	ENSP00000405931.1:p.Glu198AspfsTer21
ENST00000474381.1:n.435_436insC
ENST00000498007.1:n.826_827insC
NM_005514.6:c.560_561insC	NP_005505.2:p.Glu187AspfsTer21
XM_011514556.1:c.593_594insC	XP_011512858.1:p.Glu198AspfsTer21
XM_011514557.1:c.560_561insC	XP_011512859.1:p.Glu187AspfsTer21
XR_926175.1:n.570_571insC
NM_005514.7:c.560_561insC	NP_005505.2:p.Glu187AspfsTer21
NM_005514.8:c.560_561insC MANE Select	NP_005505.2:p.Glu187AspfsTer21