Canonical Allele Identifier: CA2678151104

Gene: HLA-DQB1

Linked Data

• gnomAD v4: 6-32659617-C-CCTAT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32659617_32659618insCTAT , CM000668.2:g.32659617_32659618insCTAT	GRCh38
NC_000006.11:g.32627394_32627395insCTAT , CM000668.1:g.32627394_32627395insCTAT	GRCh37
NC_000006.10:g.32735372_32735373insCTAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000434651.7:c.*618_*619insATAG MANE Select	ENSP00000407332.2:n.*618_*619insATAG
ENST00000374943.8:c.*618_*619insATAG	ENSP00000364080.4:n.*618_*619insATAG
ENST00000399079.7:c.*618_*619insATAG	ENSP00000382029.3:n.*618_*619insATAG
ENST00000399082.7:c.*618_*619insATAG	ENSP00000382032.3:n.*618_*619insATAG
ENST00000399084.5:c.*618_*619insATAG	ENSP00000382034.1:n.*618_*619insATAG
ENST00000434651.6:c.*618_*619insATAG	ENSP00000407332.2:n.*618_*619insATAG
ENST00000487676.1:n.4493_4494insATAG
NM_001243961.1:c.*618_*619insATAG	NP_001230890.1:n.*618_*619insATAG
NM_002123.4:c.*618_*619insATAG	NP_002114.3:n.*618_*619insATAG
NM_001243961.2:c.*618_*619insATAG	NP_001230890.1:n.*618_*619insATAG
NM_002123.5:c.*618_*619insATAG MANE Select	NP_002114.3:n.*618_*619insATAG