Canonical Allele Identifier: CA2677957890
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357092dup , CM000668.2:g.31357092dup GRCh38
NC_000006.11:g.31324869dup , CM000668.1:g.31324869dup GRCh37
NC_000006.10:g.31432848dup NCBI36
NG_023187.1:g.5121dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1540dup
ENST00000481849.6:n.1540dup
ENST00000497377.6:n.1540dup
ENST00000640094.2:c.67dup ENSP00000491275.2:p.Trp23LeufsTer?
ENST00000696558.1:c.67dup ENSP00000512716.1:p.Trp23LeufsTer?
ENST00000696559.1:c.67dup ENSP00000512717.1:p.Trp23LeufsTer?
ENST00000696560.1:c.67dup ENSP00000512718.1:p.Trp23LeufsTer?
ENST00000696561.1:c.67dup ENSP00000512719.1:p.Trp23LeufsTer?
ENST00000696562.1:c.67dup ENSP00000512720.1:p.Trp23LeufsTer?
ENST00000412585.7:c.67dup MANE Select ENSP00000399168.2:p.Trp23LeufsTer?
ENST00000412585.6:c.67dup ENSP00000399168.2:p.Trp23LeufsTer?
ENST00000434333.1:c.-29dup ENSP00000405931.1:n.-29dup
ENST00000498007.1:n.88dup
ENST00000603274.1:n.446dup
NM_005514.6:c.67dup NP_005505.2:p.Trp23LeufsTer?
XM_011514557.1:c.67dup XP_011512859.1:p.Trp23LeufsTer?
XR_926175.1:n.77dup
NM_005514.7:c.67dup NP_005505.2:p.Trp23LeufsTer?
NM_005514.8:c.67dup MANE Select NP_005505.2:p.Trp23LeufsTer?