Canonical Allele Identifier: CA1087464774
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355201del , CM000668.2:g.31355201del GRCh38
NC_000006.11:g.31322978del , CM000668.1:g.31322978del GRCh37
NC_000006.10:g.31430957del NCBI36
NG_023187.1:g.7015del

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.2968del
ENST00000481849.6:n.2487del
ENST00000497377.6:n.2394del
ENST00000640094.2:c.895+119del ENSP00000491275.2:n.895+119del
ENST00000696558.1:c.990del ENSP00000512716.1:n.990del
ENST00000696559.1:c.921del ENSP00000512717.1:p.Ile308SerfsTer11
ENST00000696560.1:c.921del ENSP00000512718.1:p.Ile308SerfsTer11
ENST00000696561.1:c.921del ENSP00000512719.1:p.Ile308SerfsTer11
ENST00000696562.1:c.921del ENSP00000512720.1:p.Ile308SerfsTer11
ENST00000412585.7:c.921del MANE Select ENSP00000399168.2:p.Ile308SerfsTer11
ENST00000640094.1:c.88+119del ENSP00000491275.1:n.88+119del
ENST00000412585.6:c.921del ENSP00000399168.2:p.Ile308SerfsTer11
ENST00000463574.1:n.512del
NM_005514.6:c.921del NP_005505.2:p.Ile308SerfsTer11
XM_011514556.1:c.954del XP_011512858.1:p.Ile319SerfsTer11
XM_011514557.1:c.895+119del XP_011512859.1:n.895+119del
XR_926175.1:n.1360del
NM_005514.7:c.921del NP_005505.2:p.Ile308SerfsTer11
NM_005514.8:c.921del MANE Select NP_005505.2:p.Ile308SerfsTer11