Canonical Allele Identifier: CA2678150989
Gene: HLA-DQB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32659590_32659591insGCAC , CM000668.2:g.32659590_32659591insGCAC GRCh38
NC_000006.11:g.32627367_32627368insGCAC , CM000668.1:g.32627367_32627368insGCAC GRCh37
NC_000006.10:g.32735345_32735346insGCAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000434651.7:c.*645_*646insGTGC MANE Select ENSP00000407332.2:n.*645_*646insGTGC
ENST00000374943.8:c.*645_*646insGTGC ENSP00000364080.4:n.*645_*646insGTGC
ENST00000399079.7:c.*645_*646insGTGC ENSP00000382029.3:n.*645_*646insGTGC
ENST00000399082.7:c.*645_*646insGTGC ENSP00000382032.3:n.*645_*646insGTGC
ENST00000399084.5:c.*645_*646insGTGC ENSP00000382034.1:n.*645_*646insGTGC
ENST00000434651.6:c.*645_*646insGTGC ENSP00000407332.2:n.*645_*646insGTGC
ENST00000487676.1:n.4520_4521insGTGC
NM_001243961.1:c.*645_*646insGTGC NP_001230890.1:n.*645_*646insGTGC
NM_002123.4:c.*645_*646insGTGC NP_002114.3:n.*645_*646insGTGC
NM_001243961.2:c.*645_*646insGTGC NP_001230890.1:n.*645_*646insGTGC
NM_002123.5:c.*645_*646insGTGC MANE Select NP_002114.3:n.*645_*646insGTGC