Canonical Allele Identifier: CA1619675052
Gene: HLA-DQB1 HGNC NCBI

Linked Data

dbSNP Id: rs9273444
gnomAD v4: 6-32659858-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32659858T>C , CM000668.2:g.32659858T>C GRCh38
NC_000006.11:g.32627635T>C , CM000668.1:g.32627635T>C GRCh37
NC_000006.10:g.32735613T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000434651.7:c.*378A>G MANE Select ENSP00000407332.2:n.*378A>G
ENST00000374943.8:c.*378A>G ENSP00000364080.4:n.*378A>G
ENST00000399079.7:c.*378A>G ENSP00000382029.3:n.*378A>G
ENST00000399082.7:c.*378A>G ENSP00000382032.3:n.*378A>G
ENST00000399084.5:c.*378A>G ENSP00000382034.1:n.*378A>G
ENST00000434651.6:c.*378A>G ENSP00000407332.2:n.*378A>G
ENST00000487676.1:n.4253A>G
NM_001243961.1:c.*378A>G NP_001230890.1:n.*378A>G
NM_002123.4:c.*378A>G NP_002114.3:n.*378A>G
NM_001243961.2:c.*378A>G NP_001230890.1:n.*378A>G
NM_002123.5:c.*378A>G MANE Select NP_002114.3:n.*378A>G