Canonical Allele Identifier: CA136953737

Gene: HLA-DQB1 HLA-DQB1-AS1

Linked Data

• dbSNP Id: rs888653196
• gnomAD v3: 6-32660162-T-C
• gnomAD v4: 6-32660162-T-C
• MyVariant Identifiers: chr6:g.32627939T>C (hg19) ; chr6:g.32660162T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32660162T>C , CM000668.2:g.32660162T>C	GRCh38
NC_000006.11:g.32627939T>C , CM000668.1:g.32627939T>C	GRCh37
NC_000006.10:g.32735917T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000434651.7:c.*74A>G (HLA-DQB1) MANE Select	ENSP00000407332.2:n.*74A>G
ENST00000374943.8:c.*74A>G (HLA-DQB1)	ENSP00000364080.4:n.*74A>G
ENST00000399079.7:c.*74A>G (HLA-DQB1)	ENSP00000382029.3:n.*74A>G
ENST00000399082.7:c.*74A>G (HLA-DQB1)	ENSP00000382032.3:n.*74A>G
ENST00000399084.5:c.*74A>G (HLA-DQB1)	ENSP00000382034.1:n.*74A>G
ENST00000434651.6:c.*74A>G (HLA-DQB1)	ENSP00000407332.2:n.*74A>G
ENST00000443574.1:n.98-65A>G (HLA-DQB1)
ENST00000460185.1:n.152A>G (HLA-DQB1)
ENST00000484729.2:c.*286A>G (HLA-DQB1)	ENSP00000436686.1:n.*286A>G
ENST00000487676.1:n.3949A>G (HLA-DQB1)
NM_001243961.1:c.*74A>G (HLA-DQB1)	NP_001230890.1:n.*74A>G
NM_002123.4:c.*74A>G (HLA-DQB1)	NP_002114.3:n.*74A>G
NR_133907.1:n.177+106T>C (HLA-DQB1-AS1)
NM_001243961.2:c.*74A>G (HLA-DQB1)	NP_001230890.1:n.*74A>G
NM_002123.5:c.*74A>G (HLA-DQB1) MANE Select	NP_002114.3:n.*74A>G