Canonical Allele Identifier: CA1087615978

Gene: HLA-DQB1

Linked Data

• gnomAD v3: 6-32659617-C-CTTGT
• gnomAD v4: 6-32659617-C-CTTGT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32659617_32659618insTTGT , CM000668.2:g.32659617_32659618insTTGT	GRCh38
NC_000006.11:g.32627394_32627395insTTGT , CM000668.1:g.32627394_32627395insTTGT	GRCh37
NC_000006.10:g.32735372_32735373insTTGT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000434651.7:c.*618_*619insACAA MANE Select	ENSP00000407332.2:n.*618_*619insACAA
ENST00000374943.8:c.*618_*619insACAA	ENSP00000364080.4:n.*618_*619insACAA
ENST00000399079.7:c.*618_*619insACAA	ENSP00000382029.3:n.*618_*619insACAA
ENST00000399082.7:c.*618_*619insACAA	ENSP00000382032.3:n.*618_*619insACAA
ENST00000399084.5:c.*618_*619insACAA	ENSP00000382034.1:n.*618_*619insACAA
ENST00000434651.6:c.*618_*619insACAA	ENSP00000407332.2:n.*618_*619insACAA
ENST00000487676.1:n.4493_4494insACAA
NM_001243961.1:c.*618_*619insACAA	NP_001230890.1:n.*618_*619insACAA
NM_002123.4:c.*618_*619insACAA	NP_002114.3:n.*618_*619insACAA
NM_001243961.2:c.*618_*619insACAA	NP_001230890.1:n.*618_*619insACAA
NM_002123.5:c.*618_*619insACAA MANE Select	NP_002114.3:n.*618_*619insACAA