Canonical Allele Identifier: CA1619674989
Gene: HLA-DQB1 HGNC NCBI

Linked Data

dbSNP Id: rs1782806017
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32659750_32659751insACA , CM000668.2:g.32659750_32659751insACA GRCh38
NC_000006.11:g.32627527_32627528insACA , CM000668.1:g.32627527_32627528insACA GRCh37
NC_000006.10:g.32735505_32735506insACA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000434651.7:c.*485_*486insTGT MANE Select ENSP00000407332.2:n.*485_*486insTGT
ENST00000374943.8:c.*485_*486insTGT ENSP00000364080.4:n.*485_*486insTGT
ENST00000399079.7:c.*485_*486insTGT ENSP00000382029.3:n.*485_*486insTGT
ENST00000399082.7:c.*485_*486insTGT ENSP00000382032.3:n.*485_*486insTGT
ENST00000399084.5:c.*485_*486insTGT ENSP00000382034.1:n.*485_*486insTGT
ENST00000434651.6:c.*485_*486insTGT ENSP00000407332.2:n.*485_*486insTGT
ENST00000487676.1:n.4360_4361insTGT
NM_001243961.1:c.*485_*486insTGT NP_001230890.1:n.*485_*486insTGT
NM_002123.4:c.*485_*486insTGT NP_002114.3:n.*485_*486insTGT
NM_001243961.2:c.*485_*486insTGT NP_001230890.1:n.*485_*486insTGT
NM_002123.5:c.*485_*486insTGT MANE Select NP_002114.3:n.*485_*486insTGT
Search 100 bp 5'
Search 100 bp 3'