Canonical Allele Identifier: CA1087465329
Gene: HLA-B HGNC NCBI

Linked Data

gnomAD v3: 6-31355397-AC-A
gnomAD v4: 6-31355397-AC-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355399del , CM000668.2:g.31355399del GRCh38
NC_000006.11:g.31323176del , CM000668.1:g.31323176del GRCh37
NC_000006.10:g.31431155del NCBI36
NG_023187.1:g.6815del

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.2861del
ENST00000481849.6:n.2287del
ENST00000497377.6:n.2287del
ENST00000640094.2:c.814del ENSP00000491275.2:p.Val272TrpfsTer25
ENST00000696558.1:c.883del ENSP00000512716.1:n.883del
ENST00000696559.1:c.814del ENSP00000512717.1:p.Val272TrpfsTer25
ENST00000696560.1:c.814del ENSP00000512718.1:p.Val272TrpfsTer25
ENST00000696561.1:c.814del ENSP00000512719.1:p.Val272TrpfsTer25
ENST00000696562.1:c.814del ENSP00000512720.1:p.Val272TrpfsTer25
ENST00000412585.7:c.814del MANE Select ENSP00000399168.2:p.Val272TrpfsTer25
ENST00000640094.1:c.7del ENSP00000491275.1:p.Val3TrpfsTer25
ENST00000412585.6:c.814del ENSP00000399168.2:p.Val272TrpfsTer25
ENST00000463574.1:n.405del
ENST00000498007.1:n.1080del
NM_005514.6:c.814del NP_005505.2:p.Val272TrpfsTer25
XM_011514556.1:c.847del XP_011512858.1:p.Val283TrpfsTer25
XM_011514557.1:c.814del XP_011512859.1:p.Val272TrpfsTer25
XR_926175.1:n.1253del
NM_005514.7:c.814del NP_005505.2:p.Val272TrpfsTer25
NM_005514.8:c.814del MANE Select NP_005505.2:p.Val272TrpfsTer25
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