Canonical Allele Identifier: CA1619674992
Gene: HLA-DQB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32659752_32659753delinsCA , CM000668.2:g.32659752_32659753delinsCA GRCh38
NC_000006.11:g.32627529_32627530delinsCA , CM000668.1:g.32627529_32627530delinsCA GRCh37
NC_000006.10:g.32735507_32735508delinsCA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000434651.7:c.*483_*484delinsTG MANE Select ENSP00000407332.2:n.*483_*484delinsTG
ENST00000374943.8:c.*483_*484delinsTG ENSP00000364080.4:n.*483_*484delinsTG
ENST00000399079.7:c.*483_*484delinsTG ENSP00000382029.3:n.*483_*484delinsTG
ENST00000399082.7:c.*483_*484delinsTG ENSP00000382032.3:n.*483_*484delinsTG
ENST00000399084.5:c.*483_*484delinsTG ENSP00000382034.1:n.*483_*484delinsTG
ENST00000434651.6:c.*483_*484delinsTG ENSP00000407332.2:n.*483_*484delinsTG
ENST00000487676.1:n.4358_4359delinsTG
NM_001243961.1:c.*483_*484delinsTG NP_001230890.1:n.*483_*484delinsTG
NM_002123.4:c.*483_*484delinsTG NP_002114.3:n.*483_*484delinsTG
NM_001243961.2:c.*483_*484delinsTG NP_001230890.1:n.*483_*484delinsTG
NM_002123.5:c.*483_*484delinsTG MANE Select NP_002114.3:n.*483_*484delinsTG