Canonical Allele Identifier: CA12266529
Gene: HLA-DQB1 HGNC NCBI
HLA-DQB1-AS1 HGNC NCBI
MyVariant.info:
GRCh38 chr6:g.32659970A>G
GRCh37 chr6:g.32627747A>G
gnomAD v2:
6:32627747 A / G
gnomAD v3:
6:32659970 A / G
gnomAD v4:
chr6-32659970-A-G
Joint Max Group AF 0.79524261 (SAS)
Genomes Max Group AF 0.89014807 (EAS)
Exomes Max Group AF 0.72878257 (SAS)
dbSNP:
1049225
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32659970A>G , CM000668.2:g.32659970A>G GRCh38
NC_000006.11:g.32627747A>G , CM000668.1:g.32627747A>G GRCh37
NC_000006.10:g.32735725A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000434651.7:c.*266T>C (HLA-DQB1) MANE Select ENSP00000407332.2:n.*266T>C
ENST00000374943.8:c.*266T>C (HLA-DQB1) ENSP00000364080.4:n.*266T>C
ENST00000399079.7:c.*266T>C (HLA-DQB1) ENSP00000382029.3:n.*266T>C
ENST00000399082.7:c.*266T>C (HLA-DQB1) ENSP00000382032.3:n.*266T>C
ENST00000399084.5:c.*266T>C (HLA-DQB1) ENSP00000382034.1:n.*266T>C
ENST00000434651.6:c.*266T>C (HLA-DQB1) ENSP00000407332.2:n.*266T>C
ENST00000443574.1:n.225T>C (HLA-DQB1)
ENST00000460185.1:n.344T>C (HLA-DQB1)
ENST00000487676.1:n.4141T>C (HLA-DQB1)
NM_001243961.1:c.*266T>C (HLA-DQB1) NP_001230890.1:n.*266T>C
NM_002123.4:c.*266T>C (HLA-DQB1) NP_002114.3:n.*266T>C
NR_133907.1:n.91A>G (HLA-DQB1-AS1)
NM_001243961.2:c.*266T>C (HLA-DQB1) NP_001230890.1:n.*266T>C
NM_002123.5:c.*266T>C (HLA-DQB1) MANE Select NP_002114.3:n.*266T>C
Search 100 bp 5'
Search 100 bp 3'