Canonical Allele Identifier: CA449744312

Gene: HLA-DQB1 HLA-DQB1-AS1

Linked Data

• dbSNP Id: rs1049219
• gnomAD v4: 6-32659986-A-C
• MyVariant Identifiers: chr6:g.32627763A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32659986A>C , CM000668.2:g.32659986A>C	GRCh38
NC_000006.11:g.32627763A>C , CM000668.1:g.32627763A>C	GRCh37
NC_000006.10:g.32735741A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000434651.7:c.*250T>G (HLA-DQB1) MANE Select	ENSP00000407332.2:n.*250T>G
ENST00000374943.8:c.*250T>G (HLA-DQB1)	ENSP00000364080.4:n.*250T>G
ENST00000399079.7:c.*250T>G (HLA-DQB1)	ENSP00000382029.3:n.*250T>G
ENST00000399082.7:c.*250T>G (HLA-DQB1)	ENSP00000382032.3:n.*250T>G
ENST00000399084.5:c.*250T>G (HLA-DQB1)	ENSP00000382034.1:n.*250T>G
ENST00000434651.6:c.*250T>G (HLA-DQB1)	ENSP00000407332.2:n.*250T>G
ENST00000443574.1:n.209T>G (HLA-DQB1)
ENST00000460185.1:n.328T>G (HLA-DQB1)
ENST00000487676.1:n.4125T>G (HLA-DQB1)
NM_001243961.1:c.*250T>G (HLA-DQB1)	NP_001230890.1:n.*250T>G
NM_002123.4:c.*250T>G (HLA-DQB1)	NP_002114.3:n.*250T>G
NR_133907.1:n.107A>C (HLA-DQB1-AS1)
NM_001243961.2:c.*250T>G (HLA-DQB1)	NP_001230890.1:n.*250T>G
NM_002123.5:c.*250T>G (HLA-DQB1) MANE Select	NP_002114.3:n.*250T>G