Canonical Allele Identifier: CA3711832

Gene: HLA-B

Linked Data

• dbSNP Id: rs761978020
• ExAC: 6:31324598 C / CGCGA
• gnomAD v2: 6-31324598-C-CGCGA
• MyVariant Identifiers: chr6:g.31324598_31324599insGCGA (hg19) ; chr6:g.31324599_31324604delinsGCGATCCTCT (hg19) ; chr6:g.31356821_31356822insGCGA (hg38) ; chr6:g.31356822_31356827delinsGCGATCCTCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356821_31356822insGCGA , CM000668.2:g.31356821_31356822insGCGA	GRCh38
NC_000006.11:g.31324598_31324599insGCGA , CM000668.1:g.31324598_31324599insGCGA	GRCh37
NC_000006.10:g.31432577_31432578insGCGA	NCBI36
NG_023187.1:g.5391_5392insTCGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1682_1683insTCGC
ENST00000481849.6:n.1682_1683insTCGC
ENST00000497377.6:n.1682_1683insTCGC
ENST00000640094.2:c.209_210insTCGC	ENSP00000491275.2:p.Glu70AspfsTer30
ENST00000696558.1:c.209_210insTCGC	ENSP00000512716.1:p.Glu70AspfsTer30
ENST00000696559.1:c.209_210insTCGC	ENSP00000512717.1:p.Glu70AspfsTer30
ENST00000696560.1:c.209_210insTCGC	ENSP00000512718.1:p.Glu70AspfsTer30
ENST00000696561.1:c.209_210insTCGC	ENSP00000512719.1:p.Glu70AspfsTer30
ENST00000696562.1:c.209_210insTCGC	ENSP00000512720.1:p.Glu70AspfsTer30
ENST00000412585.7:c.209_210insTCGC MANE Select	ENSP00000399168.2:p.Glu70AspfsTer30
ENST00000412585.6:c.209_210insTCGC	ENSP00000399168.2:p.Glu70AspfsTer30
ENST00000434333.1:c.242_243insTCGC	ENSP00000405931.1:p.Glu81AspfsTer30
ENST00000474381.1:n.84_85insTCGC
ENST00000498007.1:n.230_231insTCGC
ENST00000603274.1:n.175_176insGCGA
NM_005514.6:c.209_210insTCGC	NP_005505.2:p.Glu70AspfsTer30
XM_011514556.1:c.242_243insTCGC	XP_011512858.1:p.Glu81AspfsTer30
XM_011514557.1:c.209_210insTCGC	XP_011512859.1:p.Glu70AspfsTer30
XR_926175.1:n.219_220insTCGC
NM_005514.7:c.209_210insTCGC	NP_005505.2:p.Glu70AspfsTer30
NM_005514.8:c.209_210insTCGC MANE Select	NP_005505.2:p.Glu70AspfsTer30