Canonical Allele Identifier: CA900072
Gene: IL23R HGNC NCBI

Linked Data

dbSNP Id: rs751643545

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67259149_67259155del , CM000663.2:g.67259149_67259155del GRCh38
NC_000001.10:g.67724832_67724838del , CM000663.1:g.67724832_67724838del GRCh37
NC_000001.9:g.67497420_67497426del NCBI36
NG_011498.1:g.97664_97670del

Transcript Alleles

HGVS Amino-acid change
ENST00000347310.10:c.*21_*27del MANE Select ENSP00000321345.5:n.*21_*27del
ENST00000637002.1:c.*21_*27del ENSP00000490340.1:n.*21_*27del
ENST00000347310.9:c.*21_*27del ENSP00000321345.5:n.*21_*27del
ENST00000395227.2:c.*21_*27del ENSP00000378652.2:n.*21_*27del
ENST00000425614.3:c.*21_*27del ENSP00000387640.2:n.*21_*27del
ENST00000473881.2:c.*737_*743del ENSP00000486667.1:n.*737_*743del
NM_144701.2:c.*21_*27del NP_653302.2:n.*21_*27del
XM_005270516.2:c.*21_*27del XP_005270573.1:n.*21_*27del
XM_011540789.1:c.*21_*27del XP_011539091.1:n.*21_*27del
XM_011540790.1:c.*21_*27del XP_011539092.1:n.*21_*27del
XM_011540791.1:c.*21_*27del XP_011539093.1:n.*21_*27del
XM_011540790.3:c.*21_*27del XP_011539092.1:n.*21_*27del
XM_011540791.3:c.*21_*27del XP_011539093.1:n.*21_*27del
NM_144701.3:c.*21_*27del MANE Select NP_653302.2:n.*21_*27del