Canonical Allele Identifier: CA2677955312
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355469del , CM000668.2:g.31355469del GRCh38
NC_000006.11:g.31323246del , CM000668.1:g.31323246del GRCh37
NC_000006.10:g.31431225del NCBI36
NG_023187.1:g.6746del

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.2792del
ENST00000481849.6:n.2218del
ENST00000497377.6:n.2218del
ENST00000640094.2:c.745del ENSP00000491275.2:p.Thr249LeufsTer?
ENST00000696558.1:c.814del ENSP00000512716.1:n.814del
ENST00000696559.1:c.745del ENSP00000512717.1:p.Thr249LeufsTer?
ENST00000696560.1:c.745del ENSP00000512718.1:p.Thr249LeufsTer?
ENST00000696561.1:c.745del ENSP00000512719.1:p.Thr249LeufsTer?
ENST00000696562.1:c.745del ENSP00000512720.1:p.Thr249LeufsTer?
ENST00000412585.7:c.745del MANE Select ENSP00000399168.2:p.Thr249LeufsTer?
ENST00000412585.6:c.745del ENSP00000399168.2:p.Thr249LeufsTer?
ENST00000463574.1:n.336del
ENST00000498007.1:n.1011del
NM_005514.6:c.745del NP_005505.2:p.Thr249LeufsTer?
XM_011514556.1:c.778del XP_011512858.1:p.Thr260LeufsTer?
XM_011514557.1:c.745del XP_011512859.1:p.Thr249LeufsTer?
XR_926175.1:n.1184del
NM_005514.7:c.745del NP_005505.2:p.Thr249LeufsTer?
NM_005514.8:c.745del MANE Select NP_005505.2:p.Thr249LeufsTer?