Canonical Allele Identifier: CA3711829
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs761978020

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356821_31356822insGCCA , CM000668.2:g.31356821_31356822insGCCA GRCh38
NC_000006.11:g.31324598_31324599insGCCA , CM000668.1:g.31324598_31324599insGCCA GRCh37
NC_000006.10:g.31432577_31432578insGCCA NCBI36
NG_023187.1:g.5391_5392insTGGC

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.1682_1683insTGGC
ENST00000481849.6:n.1682_1683insTGGC
ENST00000497377.6:n.1682_1683insTGGC
ENST00000640094.2:c.209_210insTGGC ENSP00000491275.2:p.Glu70AspfsTer30
ENST00000696558.1:c.209_210insTGGC ENSP00000512716.1:p.Glu70AspfsTer30
ENST00000696559.1:c.209_210insTGGC ENSP00000512717.1:p.Glu70AspfsTer30
ENST00000696560.1:c.209_210insTGGC ENSP00000512718.1:p.Glu70AspfsTer30
ENST00000696561.1:c.209_210insTGGC ENSP00000512719.1:p.Glu70AspfsTer30
ENST00000696562.1:c.209_210insTGGC ENSP00000512720.1:p.Glu70AspfsTer30
ENST00000412585.7:c.209_210insTGGC MANE Select ENSP00000399168.2:p.Glu70AspfsTer30
ENST00000412585.6:c.209_210insTGGC ENSP00000399168.2:p.Glu70AspfsTer30
ENST00000434333.1:c.242_243insTGGC ENSP00000405931.1:p.Glu81AspfsTer30
ENST00000474381.1:n.84_85insTGGC
ENST00000498007.1:n.230_231insTGGC
ENST00000603274.1:n.175_176insGCCA
NM_005514.6:c.209_210insTGGC NP_005505.2:p.Glu70AspfsTer30
XM_011514556.1:c.242_243insTGGC XP_011512858.1:p.Glu81AspfsTer30
XM_011514557.1:c.209_210insTGGC XP_011512859.1:p.Glu70AspfsTer30
XR_926175.1:n.219_220insTGGC
NM_005514.7:c.209_210insTGGC NP_005505.2:p.Glu70AspfsTer30
NM_005514.8:c.209_210insTGGC MANE Select NP_005505.2:p.Glu70AspfsTer30