Canonical Allele Identifier: CA12426811

Gene: HLA-DQB1

Linked Data

• dbSNP Id: rs9273429
• gnomAD v2: 6-32627456-G-A
• gnomAD v3: 6-32659679-G-A
• gnomAD v4: 6-32659679-G-A
• MyVariant Identifiers: chr6:g.32627456G>A (hg19) ; chr6:g.32659679G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32659679G>A , CM000668.2:g.32659679G>A	GRCh38
NC_000006.11:g.32627456G>A , CM000668.1:g.32627456G>A	GRCh37
NC_000006.10:g.32735434G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000434651.7:c.*557C>T MANE Select	ENSP00000407332.2:n.*557C>T
ENST00000374943.8:c.*557C>T	ENSP00000364080.4:n.*557C>T
ENST00000399079.7:c.*557C>T	ENSP00000382029.3:n.*557C>T
ENST00000399082.7:c.*557C>T	ENSP00000382032.3:n.*557C>T
ENST00000399084.5:c.*557C>T	ENSP00000382034.1:n.*557C>T
ENST00000434651.6:c.*557C>T	ENSP00000407332.2:n.*557C>T
ENST00000487676.1:n.4432C>T
NM_001243961.1:c.*557C>T	NP_001230890.1:n.*557C>T
NM_002123.4:c.*557C>T	NP_002114.3:n.*557C>T
NM_001243961.2:c.*557C>T	NP_001230890.1:n.*557C>T
NM_002123.5:c.*557C>T MANE Select	NP_002114.3:n.*557C>T