Canonical Allele Identifier: CA340728690
Gene: IL23R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67258785T>G , CM000663.2:g.67258785T>G GRCh38
NC_000001.10:g.67724468T>G , CM000663.1:g.67724468T>G GRCh37
NC_000001.9:g.67497056T>G NCBI36
NG_011498.1:g.97300T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000697149.1:c.1386T>G ENSP00000513138.1:n.1386T>G
ENST00000697150.1:c.1444T>G ENSP00000513139.1:n.1444T>G
ENST00000697151.1:c.1377T>G ENSP00000513140.1:n.1377T>G
ENST00000697164.1:c.1457T>G ENSP00000513153.1:p.Leu486Ter
ENST00000697165.1:c.1244T>G ENSP00000513154.1:p.Leu415Ter
ENST00000347310.10:c.1547T>G MANE Select ENSP00000321345.5:p.Leu516Ter
ENST00000637002.1:c.938T>G ENSP00000490340.1:p.Leu313Ter
ENST00000347310.9:c.1547T>G ENSP00000321345.5:p.Leu516Ter
ENST00000395227.2:c.341T>G ENSP00000378652.2:p.Leu114Ter
ENST00000425614.3:c.782T>G ENSP00000387640.2:p.Leu261Ter
ENST00000473881.2:c.*373T>G ENSP00000486667.1:n.*373T>G
NM_144701.2:c.1547T>G NP_653302.2:p.Leu516Ter
XM_005270516.2:c.785T>G XP_005270573.1:p.Leu262Ter
XM_011540789.1:c.1637T>G XP_011539091.1:p.Leu546Ter
XM_011540790.1:c.1547T>G XP_011539092.1:p.Leu516Ter
XM_011540791.1:c.1547T>G XP_011539093.1:p.Leu516Ter
XM_011540790.3:c.1547T>G XP_011539092.1:p.Leu516Ter
XM_011540791.3:c.1547T>G XP_011539093.1:p.Leu516Ter
XR_001736993.1:n.1627T>G
NM_144701.3:c.1547T>G MANE Select NP_653302.2:p.Leu516Ter