Canonical Allele Identifier: CA2711130244
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs759615853

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356492_31356496dup , CM000668.2:g.31356492_31356496dup GRCh38
NC_000006.11:g.31324269_31324273dup , CM000668.1:g.31324269_31324273dup GRCh37
NC_000006.10:g.31432248_31432252dup NCBI36
NG_023187.1:g.5719_5723dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1817-52_1817-48dup
ENST00000481849.6:n.1817-52_1817-48dup
ENST00000497377.6:n.1817-52_1817-48dup
ENST00000640094.2:c.344-52_344-48dup ENSP00000491275.2:n.344-52_344-48dup
ENST00000696558.1:c.344-52_344-48dup ENSP00000512716.1:n.344-52_344-48dup
ENST00000696559.1:c.344-52_344-48dup ENSP00000512717.1:n.344-52_344-48dup
ENST00000696560.1:c.344-52_344-48dup ENSP00000512718.1:n.344-52_344-48dup
ENST00000696561.1:c.344-52_344-48dup ENSP00000512719.1:n.344-52_344-48dup
ENST00000696562.1:c.344-52_344-48dup ENSP00000512720.1:n.344-52_344-48dup
ENST00000412585.7:c.344-52_344-48dup MANE Select ENSP00000399168.2:n.344-52_344-48dup
ENST00000412585.6:c.344-52_344-48dup ENSP00000399168.2:n.344-52_344-48dup
ENST00000434333.1:c.377-52_377-48dup ENSP00000405931.1:n.377-52_377-48dup
ENST00000474381.1:n.219-52_219-48dup
ENST00000498007.1:n.558_562dup
NM_005514.6:c.344-52_344-48dup NP_005505.2:n.344-52_344-48dup
XM_011514556.1:c.377-52_377-48dup XP_011512858.1:n.377-52_377-48dup
XM_011514557.1:c.344-52_344-48dup XP_011512859.1:n.344-52_344-48dup
XR_926175.1:n.354-52_354-48dup
NM_005514.7:c.344-52_344-48dup NP_005505.2:n.344-52_344-48dup
NM_005514.8:c.344-52_344-48dup MANE Select NP_005505.2:n.344-52_344-48dup