Canonical Allele Identifier: CA566697672

Gene: HLA-DQB1 HLA-DQB1-AS1

Linked Data

• dbSNP Id: rs1554163327
• gnomAD v2: 6-32627850-TGG-T
• gnomAD v3: 6-32660073-TGG-T
• gnomAD v4: 6-32660073-TGG-T
• MyVariant Identifiers: chr6:g.32627851_32627852del (hg19) ; chr6:g.32660074_32660075del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32660076_32660077del , CM000668.2:g.32660076_32660077del	GRCh38
NC_000006.11:g.32627853_32627854del , CM000668.1:g.32627853_32627854del	GRCh37
NC_000006.10:g.32735831_32735832del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000434651.7:c.*161_*162del (HLA-DQB1) MANE Select	ENSP00000407332.2:n.*161_*162del
ENST00000374943.8:c.*161_*162del (HLA-DQB1)	ENSP00000364080.4:n.*161_*162del
ENST00000399079.7:c.*161_*162del (HLA-DQB1)	ENSP00000382029.3:n.*161_*162del
ENST00000399082.7:c.*161_*162del (HLA-DQB1)	ENSP00000382032.3:n.*161_*162del
ENST00000399084.5:c.*161_*162del (HLA-DQB1)	ENSP00000382034.1:n.*161_*162del
ENST00000434651.6:c.*161_*162del (HLA-DQB1)	ENSP00000407332.2:n.*161_*162del
ENST00000443574.1:n.120_121del (HLA-DQB1)
ENST00000460185.1:n.239_240del (HLA-DQB1)
ENST00000487676.1:n.4036_4037del (HLA-DQB1)
NM_001243961.1:c.*161_*162del (HLA-DQB1)	NP_001230890.1:n.*161_*162del
NM_002123.4:c.*161_*162del (HLA-DQB1)	NP_002114.3:n.*161_*162del
NR_133907.1:n.177+20_177+21del (HLA-DQB1-AS1)
NM_001243961.2:c.*161_*162del (HLA-DQB1)	NP_001230890.1:n.*161_*162del
NM_002123.5:c.*161_*162del (HLA-DQB1) MANE Select	NP_002114.3:n.*161_*162del