Canonical Allele Identifier: CA2677954927
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355113_31355117del , CM000668.2:g.31355113_31355117del GRCh38
NC_000006.11:g.31322890_31322894del , CM000668.1:g.31322890_31322894del GRCh37
NC_000006.10:g.31430869_31430873del NCBI36
NG_023187.1:g.7097_7101del

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.3050_3054del
ENST00000481849.6:n.2569_2573del
ENST00000497377.6:n.2476_2480del
ENST00000640094.2:c.895+201_895+205del ENSP00000491275.2:n.895+201_895+205del
ENST00000696558.1:c.1072_1076del ENSP00000512716.1:n.1072_1076del
ENST00000696559.1:c.1003_1007del ENSP00000512717.1:p.Lys335PhefsTer21
ENST00000696560.1:c.1003_1007del ENSP00000512718.1:p.Lys335PhefsTer21
ENST00000696561.1:c.1003_1007del ENSP00000512719.1:p.Lys335PhefsTer21
ENST00000696562.1:c.1003_1007del ENSP00000512720.1:p.Lys335PhefsTer21
ENST00000412585.7:c.1003_1007del MANE Select ENSP00000399168.2:p.Lys335PhefsTer21
ENST00000640094.1:c.88+201_88+205del ENSP00000491275.1:n.88+201_88+205del
ENST00000412585.6:c.1003_1007del ENSP00000399168.2:p.Lys335PhefsTer21
NM_005514.6:c.1003_1007del NP_005505.2:p.Lys335PhefsTer21
XM_011514556.1:c.1036_1040del XP_011512858.1:p.Lys346PhefsTer21
XM_011514557.1:c.895+201_895+205del XP_011512859.1:n.895+201_895+205del
XR_926175.1:n.1442_1446del
NM_005514.7:c.1003_1007del NP_005505.2:p.Lys335PhefsTer21
NM_005514.8:c.1003_1007del MANE Select NP_005505.2:p.Lys335PhefsTer21