Canonical Allele Identifier: CA566697675

Gene: HLA-DQB1 HLA-DQB1-AS1

Linked Data

• dbSNP Id: rs1341028651
• gnomAD v2: 6-32627918-G-A
• gnomAD v3: 6-32660141-G-A
• gnomAD v4: 6-32660141-G-A
• MyVariant Identifiers: chr6:g.32627918G>A (hg19) ; chr6:g.32660141G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32660141G>A , CM000668.2:g.32660141G>A	GRCh38
NC_000006.11:g.32627918G>A , CM000668.1:g.32627918G>A	GRCh37
NC_000006.10:g.32735896G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000434651.7:c.*95C>T (HLA-DQB1) MANE Select	ENSP00000407332.2:n.*95C>T
ENST00000374943.8:c.*95C>T (HLA-DQB1)	ENSP00000364080.4:n.*95C>T
ENST00000399079.7:c.*95C>T (HLA-DQB1)	ENSP00000382029.3:n.*95C>T
ENST00000399082.7:c.*95C>T (HLA-DQB1)	ENSP00000382032.3:n.*95C>T
ENST00000399084.5:c.*95C>T (HLA-DQB1)	ENSP00000382034.1:n.*95C>T
ENST00000434651.6:c.*95C>T (HLA-DQB1)	ENSP00000407332.2:n.*95C>T
ENST00000443574.1:n.98-44C>T (HLA-DQB1)
ENST00000460185.1:n.173C>T (HLA-DQB1)
ENST00000484729.2:c.*307C>T (HLA-DQB1)	ENSP00000436686.1:n.*307C>T
ENST00000487676.1:n.3970C>T (HLA-DQB1)
NM_001243961.1:c.*95C>T (HLA-DQB1)	NP_001230890.1:n.*95C>T
NM_002123.4:c.*95C>T (HLA-DQB1)	NP_002114.3:n.*95C>T
NR_133907.1:n.177+85G>A (HLA-DQB1-AS1)
NM_001243961.2:c.*95C>T (HLA-DQB1)	NP_001230890.1:n.*95C>T
NM_002123.5:c.*95C>T (HLA-DQB1) MANE Select	NP_002114.3:n.*95C>T