Canonical Allele Identifier: CA1619112505
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs1767048328

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356605_31356614dup , CM000668.2:g.31356605_31356614dup GRCh38
NC_000006.11:g.31324382_31324391dup , CM000668.1:g.31324382_31324391dup GRCh37
NC_000006.10:g.31432361_31432370dup NCBI36
NG_023187.1:g.5599_5608dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1816+74_1816+83dup
ENST00000481849.6:n.1816+74_1816+83dup
ENST00000497377.6:n.1816+74_1816+83dup
ENST00000640094.2:c.343+74_343+83dup ENSP00000491275.2:n.343+74_343+83dup
ENST00000696558.1:c.343+74_343+83dup ENSP00000512716.1:n.343+74_343+83dup
ENST00000696559.1:c.343+74_343+83dup ENSP00000512717.1:n.343+74_343+83dup
ENST00000696560.1:c.343+74_343+83dup ENSP00000512718.1:n.343+74_343+83dup
ENST00000696561.1:c.343+74_343+83dup ENSP00000512719.1:n.343+74_343+83dup
ENST00000696562.1:c.343+74_343+83dup ENSP00000512720.1:n.343+74_343+83dup
ENST00000412585.7:c.343+74_343+83dup MANE Select ENSP00000399168.2:n.343+74_343+83dup
ENST00000412585.6:c.343+74_343+83dup ENSP00000399168.2:n.343+74_343+83dup
ENST00000434333.1:c.376+74_376+83dup ENSP00000405931.1:n.376+74_376+83dup
ENST00000474381.1:n.218+74_218+83dup
ENST00000498007.1:n.438_447dup
NM_005514.6:c.343+74_343+83dup NP_005505.2:n.343+74_343+83dup
XM_011514556.1:c.376+74_376+83dup XP_011512858.1:n.376+74_376+83dup
XM_011514557.1:c.343+74_343+83dup XP_011512859.1:n.343+74_343+83dup
XR_926175.1:n.353+74_353+83dup
NM_005514.7:c.343+74_343+83dup NP_005505.2:n.343+74_343+83dup
NM_005514.8:c.343+74_343+83dup MANE Select NP_005505.2:n.343+74_343+83dup