Canonical Allele Identifier: CA1619674986

Gene: HLA-DQB1

Linked Data

• dbSNP Id: rs1782805517

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32659749_32659750insACA , CM000668.2:g.32659749_32659750insACA	GRCh38
NC_000006.11:g.32627526_32627527insACA , CM000668.1:g.32627526_32627527insACA	GRCh37
NC_000006.10:g.32735504_32735505insACA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000434651.7:c.*486_*487insTGT MANE Select	ENSP00000407332.2:n.*486_*487insTGT
ENST00000374943.8:c.*486_*487insTGT	ENSP00000364080.4:n.*486_*487insTGT
ENST00000399079.7:c.*486_*487insTGT	ENSP00000382029.3:n.*486_*487insTGT
ENST00000399082.7:c.*486_*487insTGT	ENSP00000382032.3:n.*486_*487insTGT
ENST00000399084.5:c.*486_*487insTGT	ENSP00000382034.1:n.*486_*487insTGT
ENST00000434651.6:c.*486_*487insTGT	ENSP00000407332.2:n.*486_*487insTGT
ENST00000487676.1:n.4361_4362insTGT
NM_001243961.1:c.*486_*487insTGT	NP_001230890.1:n.*486_*487insTGT
NM_002123.4:c.*486_*487insTGT	NP_002114.3:n.*486_*487insTGT
NM_001243961.2:c.*486_*487insTGT	NP_001230890.1:n.*486_*487insTGT
NM_002123.5:c.*486_*487insTGT MANE Select	NP_002114.3:n.*486_*487insTGT