Canonical Allele Identifier: CA2677954227
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31354513_31354514del , CM000668.2:g.31354513_31354514del GRCh38
NC_000006.11:g.31322290_31322291del , CM000668.1:g.31322290_31322291del GRCh37
NC_000006.10:g.31430269_31430270del NCBI36
NG_023187.1:g.7700_7701del

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.3106_3107del
ENST00000481849.6:n.3066_3067del
ENST00000497377.6:n.2973_2974del
ENST00000640094.2:c.942_943del ENSP00000491275.2:p.Gln315GlyfsTer3
ENST00000696558.1:c.1128_1129del ENSP00000512716.1:n.1128_1129del
ENST00000696559.1:c.1059_1060del ENSP00000512717.1:p.Gln354GlyfsTer3
ENST00000696560.1:c.1059_1060del ENSP00000512718.1:p.Gln354GlyfsTer3
ENST00000696561.1:c.1059_1060del ENSP00000512719.1:p.Gln354GlyfsTer3
ENST00000696562.1:c.1059_1060del ENSP00000512720.1:p.Gln354GlyfsTer3
ENST00000412585.7:c.1059_1060del MANE Select ENSP00000399168.2:p.Gln354GlyfsTer3
ENST00000640094.1:c.135_136del ENSP00000491275.1:p.Gln46GlyfsTer3
ENST00000412585.6:c.1059_1060del ENSP00000399168.2:p.Gln354GlyfsTer3
ENST00000481849.5:n.294_295del
ENST00000497377.5:n.458_459del
NM_005514.6:c.1059_1060del NP_005505.2:p.Gln354GlyfsTer3
XM_011514556.1:c.1092_1093del XP_011512858.1:p.Gln365GlyfsTer3
XM_011514557.1:c.942_943del XP_011512859.1:p.Gln315GlyfsTer3
XR_926175.1:n.1498_1499del
NM_005514.7:c.1059_1060del NP_005505.2:p.Gln354GlyfsTer3
NM_005514.8:c.1059_1060del MANE Select NP_005505.2:p.Gln354GlyfsTer3