Canonical Allele Identifier: CA136952928

Gene: HLA-DQB1

Linked Data

• dbSNP Id: rs751600196
• gnomAD v2: 6-32627389-A-G
• gnomAD v3: 6-32659612-A-G
• gnomAD v4: 6-32659612-A-G
• MyVariant Identifiers: chr6:g.32627389A>G (hg19) ; chr6:g.32659612A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32659612A>G , CM000668.2:g.32659612A>G	GRCh38
NC_000006.11:g.32627389A>G , CM000668.1:g.32627389A>G	GRCh37
NC_000006.10:g.32735367A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000434651.7:c.*624T>C MANE Select	ENSP00000407332.2:n.*624T>C
ENST00000374943.8:c.*624T>C	ENSP00000364080.4:n.*624T>C
ENST00000399079.7:c.*624T>C	ENSP00000382029.3:n.*624T>C
ENST00000399082.7:c.*624T>C	ENSP00000382032.3:n.*624T>C
ENST00000399084.5:c.*624T>C	ENSP00000382034.1:n.*624T>C
ENST00000434651.6:c.*624T>C	ENSP00000407332.2:n.*624T>C
ENST00000487676.1:n.4499T>C
NM_001243961.1:c.*624T>C	NP_001230890.1:n.*624T>C
NM_002123.4:c.*624T>C	NP_002114.3:n.*624T>C
NM_001243961.2:c.*624T>C	NP_001230890.1:n.*624T>C
NM_002123.5:c.*624T>C MANE Select	NP_002114.3:n.*624T>C