Canonical Allele Identifier: CA1619674870

Gene: HLA-DQB1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32659609_32659610delinsCT , CM000668.2:g.32659609_32659610delinsCT	GRCh38
NC_000006.11:g.32627386_32627387delinsCT , CM000668.1:g.32627386_32627387delinsCT	GRCh37
NC_000006.10:g.32735364_32735365delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000434651.7:c.*626_*627delinsAG MANE Select	ENSP00000407332.2:n.*626_*627delinsAG
ENST00000374943.8:c.*626_*627delinsAG	ENSP00000364080.4:n.*626_*627delinsAG
ENST00000399079.7:c.*626_*627delinsAG	ENSP00000382029.3:n.*626_*627delinsAG
ENST00000399082.7:c.*626_*627delinsAG	ENSP00000382032.3:n.*626_*627delinsAG
ENST00000399084.5:c.*626_*627delinsAG	ENSP00000382034.1:n.*626_*627delinsAG
ENST00000434651.6:c.*626_*627delinsAG	ENSP00000407332.2:n.*626_*627delinsAG
ENST00000487676.1:n.4501_4502delinsAG
NM_001243961.1:c.*626_*627delinsAG	NP_001230890.1:n.*626_*627delinsAG
NM_002123.4:c.*626_*627delinsAG	NP_002114.3:n.*626_*627delinsAG
NM_001243961.2:c.*626_*627delinsAG	NP_001230890.1:n.*626_*627delinsAG
NM_002123.5:c.*626_*627delinsAG MANE Select	NP_002114.3:n.*626_*627delinsAG