Canonical Allele Identifier: CA1087469264
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356713_31356714insGGAG , CM000668.2:g.31356713_31356714insGGAG GRCh38
NC_000006.11:g.31324490_31324491insGGAG , CM000668.1:g.31324490_31324491insGGAG GRCh37
NC_000006.10:g.31432469_31432470insGGAG NCBI36
NG_023187.1:g.5500_5501insTCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1791_1792insTCCC
ENST00000481849.6:n.1791_1792insTCCC
ENST00000497377.6:n.1791_1792insTCCC
ENST00000640094.2:c.318_319insTCCC ENSP00000491275.2:p.Gly107SerfsTer?
ENST00000696558.1:c.318_319insTCCC ENSP00000512716.1:p.Gly107SerfsTer?
ENST00000696559.1:c.318_319insTCCC ENSP00000512717.1:p.Gly107SerfsTer?
ENST00000696560.1:c.318_319insTCCC ENSP00000512718.1:p.Gly107SerfsTer?
ENST00000696561.1:c.318_319insTCCC ENSP00000512719.1:p.Gly107SerfsTer?
ENST00000696562.1:c.318_319insTCCC ENSP00000512720.1:p.Gly107SerfsTer?
ENST00000412585.7:c.318_319insTCCC MANE Select ENSP00000399168.2:p.Gly107SerfsTer?
ENST00000412585.6:c.318_319insTCCC ENSP00000399168.2:p.Gly107SerfsTer?
ENST00000434333.1:c.351_352insTCCC ENSP00000405931.1:p.Gly118SerfsTer?
ENST00000474381.1:n.193_194insTCCC
ENST00000498007.1:n.339_340insTCCC
ENST00000603274.1:n.67_68insGGAG
NM_005514.6:c.318_319insTCCC NP_005505.2:p.Gly107SerfsTer?
XM_011514556.1:c.351_352insTCCC XP_011512858.1:p.Gly118SerfsTer?
XM_011514557.1:c.318_319insTCCC XP_011512859.1:p.Gly107SerfsTer?
XR_926175.1:n.328_329insTCCC
NM_005514.7:c.318_319insTCCC NP_005505.2:p.Gly107SerfsTer?
NM_005514.8:c.318_319insTCCC MANE Select NP_005505.2:p.Gly107SerfsTer?