Canonical Allele Identifier: CA2770503660
Gene: HLA-B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356123del , CM000668.2:g.31356123del GRCh38
NC_000006.11:g.31323900del , CM000668.1:g.31323900del GRCh37
NC_000006.10:g.31431879del NCBI36
NG_023187.1:g.6091del

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.2137del
ENST00000481849.6:n.2092+45del
ENST00000497377.6:n.2092+45del
ENST00000640094.2:c.619+45del ENSP00000491275.2:n.619+45del
ENST00000696558.1:c.619+45del ENSP00000512716.1:n.619+45del
ENST00000696559.1:c.619+45del ENSP00000512717.1:n.619+45del
ENST00000696560.1:c.619+45del ENSP00000512718.1:n.619+45del
ENST00000696561.1:c.619+45del ENSP00000512719.1:n.619+45del
ENST00000696562.1:c.619+45del ENSP00000512720.1:n.619+45del
ENST00000412585.7:c.619+45del MANE Select ENSP00000399168.2:n.619+45del
ENST00000412585.6:c.619+45del ENSP00000399168.2:n.619+45del
ENST00000434333.1:c.652+45del ENSP00000405931.1:n.652+45del
ENST00000474381.1:n.539del
ENST00000498007.1:n.885+45del
NM_005514.6:c.619+45del NP_005505.2:n.619+45del
XM_011514556.1:c.652+45del XP_011512858.1:n.652+45del
XM_011514557.1:c.619+45del XP_011512859.1:n.619+45del
XR_926175.1:n.674del
NM_005514.7:c.619+45del NP_005505.2:n.619+45del
NM_005514.8:c.619+45del MANE Select NP_005505.2:n.619+45del