Canonical Allele Identifier: CA2522077908
Gene: HLA-B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356457_31356467del , CM000668.2:g.31356457_31356467del GRCh38
NC_000006.11:g.31324234_31324244del , CM000668.1:g.31324234_31324244del GRCh37
NC_000006.10:g.31432213_31432223del NCBI36
NG_023187.1:g.5749_5759del

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1817-22_1817-12del
ENST00000481849.6:n.1817-22_1817-12del
ENST00000497377.6:n.1817-22_1817-12del
ENST00000640094.2:c.344-22_344-12del ENSP00000491275.2:n.344-22_344-12del
ENST00000696558.1:c.344-22_344-12del ENSP00000512716.1:n.344-22_344-12del
ENST00000696559.1:c.344-22_344-12del ENSP00000512717.1:n.344-22_344-12del
ENST00000696560.1:c.344-22_344-12del ENSP00000512718.1:n.344-22_344-12del
ENST00000696561.1:c.344-22_344-12del ENSP00000512719.1:n.344-22_344-12del
ENST00000696562.1:c.344-22_344-12del ENSP00000512720.1:n.344-22_344-12del
ENST00000412585.7:c.344-22_344-12del MANE Select ENSP00000399168.2:n.344-22_344-12del
ENST00000412585.6:c.344-22_344-12del ENSP00000399168.2:n.344-22_344-12del
ENST00000434333.1:c.377-22_377-12del ENSP00000405931.1:n.377-22_377-12del
ENST00000474381.1:n.219-22_219-12del
ENST00000498007.1:n.588_598del
NM_005514.6:c.344-22_344-12del NP_005505.2:n.344-22_344-12del
XM_011514556.1:c.377-22_377-12del XP_011512858.1:n.377-22_377-12del
XM_011514557.1:c.344-22_344-12del XP_011512859.1:n.344-22_344-12del
XR_926175.1:n.354-22_354-12del
NM_005514.7:c.344-22_344-12del NP_005505.2:n.344-22_344-12del
NM_005514.8:c.344-22_344-12del MANE Select NP_005505.2:n.344-22_344-12del