Canonical Allele Identifier: CA3711951
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs137854633

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357077dup , CM000668.2:g.31357077dup GRCh38
NC_000006.11:g.31324854dup , CM000668.1:g.31324854dup GRCh37
NC_000006.10:g.31432833dup NCBI36
NG_023187.1:g.5138dup

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.1546+11dup
ENST00000481849.6:n.1546+11dup
ENST00000497377.6:n.1546+11dup
ENST00000640094.2:c.73+11dup ENSP00000491275.2:n.73+11dup
ENST00000696558.1:c.73+11dup ENSP00000512716.1:n.73+11dup
ENST00000696559.1:c.73+11dup ENSP00000512717.1:n.73+11dup
ENST00000696560.1:c.73+11dup ENSP00000512718.1:n.73+11dup
ENST00000696561.1:c.73+11dup ENSP00000512719.1:n.73+11dup
ENST00000696562.1:c.73+11dup ENSP00000512720.1:n.73+11dup
ENST00000412585.7:c.73+11dup MANE Select ENSP00000399168.2:n.73+11dup
ENST00000412585.6:c.73+11dup ENSP00000399168.2:n.73+11dup
ENST00000434333.1:c.-12dup ENSP00000405931.1:n.-12dup
ENST00000498007.1:n.94+11dup
ENST00000603274.1:n.431dup
NM_005514.6:c.73+11dup NP_005505.2:n.73+11dup
XM_011514556.1:c.-12dup XP_011512858.1:n.-12dup
XM_011514557.1:c.73+11dup XP_011512859.1:n.73+11dup
XR_926175.1:n.83+11dup
NM_005514.7:c.73+11dup NP_005505.2:n.73+11dup
NM_005514.8:c.73+11dup MANE Select NP_005505.2:n.73+11dup