Canonical Allele Identifier: CA1087615954
Gene: HLA-DQB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32659590_32659591insTCCC , CM000668.2:g.32659590_32659591insTCCC GRCh38
NC_000006.11:g.32627367_32627368insTCCC , CM000668.1:g.32627367_32627368insTCCC GRCh37
NC_000006.10:g.32735345_32735346insTCCC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000434651.7:c.*645_*646insGGGA MANE Select ENSP00000407332.2:n.*645_*646insGGGA
ENST00000374943.8:c.*645_*646insGGGA ENSP00000364080.4:n.*645_*646insGGGA
ENST00000399079.7:c.*645_*646insGGGA ENSP00000382029.3:n.*645_*646insGGGA
ENST00000399082.7:c.*645_*646insGGGA ENSP00000382032.3:n.*645_*646insGGGA
ENST00000399084.5:c.*645_*646insGGGA ENSP00000382034.1:n.*645_*646insGGGA
ENST00000434651.6:c.*645_*646insGGGA ENSP00000407332.2:n.*645_*646insGGGA
ENST00000487676.1:n.4520_4521insGGGA
NM_001243961.1:c.*645_*646insGGGA NP_001230890.1:n.*645_*646insGGGA
NM_002123.4:c.*645_*646insGGGA NP_002114.3:n.*645_*646insGGGA
NM_001243961.2:c.*645_*646insGGGA NP_001230890.1:n.*645_*646insGGGA
NM_002123.5:c.*645_*646insGGGA MANE Select NP_002114.3:n.*645_*646insGGGA