Canonical Allele Identifier: CA12266529
Gene: HLA-DQB1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1049225

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32659970A>G , CM000668.2:g.32659970A>G GRCh38
NC_000006.10:g.32735725A>G NCBI36
NC_000006.11:g.32627747A>G , CM000668.1:g.32627747A>G GRCh37

Transcript Alleles

HGVS Amino-acid change
ENST00000374943.8:c.*266T>C ENSP00000364080.4:p.=
ENST00000399079.7:c.*266T>C ENSP00000382029.3:p.=
ENST00000399082.7:c.*266T>C ENSP00000382032.3:p.=
ENST00000399084.5:c.*266T>C ENSP00000382034.1:p.=
ENST00000434651.6:c.*266T>C ENSP00000407332.2:p.=
ENST00000443574.1:n.225T>C
ENST00000460185.1:n.344T>C
ENST00000487676.1:n.4141T>C
NM_001243961.1:c.*266T>C VV NP_001230890.1:p.=
NM_002123.4:c.*266T>C VV NP_002114.3:p.=