Canonical Allele Identifier: CA2534537842
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355214del , CM000668.2:g.31355214del GRCh38
NC_000006.11:g.31322991del , CM000668.1:g.31322991del GRCh37
NC_000006.10:g.31430970del NCBI36
NG_023187.1:g.7001del

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.2954del
ENST00000481849.6:n.2473del
ENST00000497377.6:n.2380del
ENST00000640094.2:c.895+105del ENSP00000491275.2:n.895+105del
ENST00000696558.1:c.976del ENSP00000512716.1:n.976del
ENST00000696559.1:c.907del ENSP00000512717.1:p.Gln303SerfsTer16
ENST00000696560.1:c.907del ENSP00000512718.1:p.Gln303SerfsTer16
ENST00000696561.1:c.907del ENSP00000512719.1:p.Gln303SerfsTer16
ENST00000696562.1:c.907del ENSP00000512720.1:p.Gln303SerfsTer16
ENST00000412585.7:c.907del MANE Select ENSP00000399168.2:p.Gln303SerfsTer16
ENST00000640094.1:c.88+105del ENSP00000491275.1:n.88+105del
ENST00000412585.6:c.907del ENSP00000399168.2:p.Gln303SerfsTer16
ENST00000463574.1:n.498del
NM_005514.6:c.907del NP_005505.2:p.Gln303SerfsTer16
XM_011514556.1:c.940del XP_011512858.1:p.Gln314SerfsTer16
XM_011514557.1:c.895+105del XP_011512859.1:n.895+105del
XR_926175.1:n.1346del
NM_005514.7:c.907del NP_005505.2:p.Gln303SerfsTer16
NM_005514.8:c.907del MANE Select NP_005505.2:p.Gln303SerfsTer16