Canonical Allele Identifier: CA12266528
Gene: HLA-DQB1 HGNC NCBI
HLA-DQB1-AS1 HGNC NCBI
MyVariant.info:
GRCh38 chr6:g.32659937T>G
GRCh37 chr6:g.32627714T>G
gnomAD v2:
6:32627714 T / G
gnomAD v3:
6:32659937 T / G
gnomAD v4:
chr6-32659937-T-G
Joint Max Group AF 0.60409479 (AMR)
Genomes Max Group AF 0.64013773 (AMR)
Exomes Max Group AF 0.17064323 (MID)
dbSNP:
1063355
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32659937T>G , CM000668.2:g.32659937T>G GRCh38
NC_000006.11:g.32627714T>G , CM000668.1:g.32627714T>G GRCh37
NC_000006.10:g.32735692T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000434651.7:c.*299A>C (HLA-DQB1) MANE Select ENSP00000407332.2:n.*299A>C
ENST00000374943.8:c.*299A>C (HLA-DQB1) ENSP00000364080.4:n.*299A>C
ENST00000399079.7:c.*299A>C (HLA-DQB1) ENSP00000382029.3:n.*299A>C
ENST00000399082.7:c.*299A>C (HLA-DQB1) ENSP00000382032.3:n.*299A>C
ENST00000399084.5:c.*299A>C (HLA-DQB1) ENSP00000382034.1:n.*299A>C
ENST00000434651.6:c.*299A>C (HLA-DQB1) ENSP00000407332.2:n.*299A>C
ENST00000443574.1:n.258A>C (HLA-DQB1)
ENST00000460185.1:n.377A>C (HLA-DQB1)
ENST00000487676.1:n.4174A>C (HLA-DQB1)
NM_001243961.1:c.*299A>C (HLA-DQB1) NP_001230890.1:n.*299A>C
NM_002123.4:c.*299A>C (HLA-DQB1) NP_002114.3:n.*299A>C
NR_133907.1:n.58T>G (HLA-DQB1-AS1)
NM_001243961.2:c.*299A>C (HLA-DQB1) NP_001230890.1:n.*299A>C
NM_002123.5:c.*299A>C (HLA-DQB1) MANE Select NP_002114.3:n.*299A>C
Search 100 bp 5'
Search 100 bp 3'