Canonical Allele Identifier: CA1173056551
Gene: IL23R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67240248T= , CM000663.2:g.67240248T= GRCh38
NC_000001.10:g.67705931T= , CM000663.1:g.67705931T= GRCh37
NC_000001.9:g.67478519T= NCBI36
NG_011498.1:g.78763T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697148.1:c.991T= ENSP00000513137.1:n.991T=
ENST00000697149.1:c.954T= ENSP00000513138.1:n.954T=
ENST00000697150.1:c.1045+3446T= ENSP00000513139.1:n.1045+3446T=
ENST00000697151.1:c.1045+3446T= ENSP00000513140.1:n.1045+3446T=
ENST00000697152.1:c.799-15589T= ENSP00000513141.1:n.799-15589T=
ENST00000697153.1:c.795-15589T= ENSP00000513142.1:n.795-15589T=
ENST00000697154.1:c.956-18230T= ENSP00000513143.1:n.956-18230T=
ENST00000697155.1:c.649-18230T= ENSP00000513144.1:n.649-18230T=
ENST00000697156.1:c.1115T= ENSP00000513145.1:p.Leu372=
ENST00000697157.1:c.969T= ENSP00000513146.1:n.969T=
ENST00000697158.1:c.958T= ENSP00000513147.1:n.958T=
ENST00000697159.1:c.808T= ENSP00000513148.1:n.808T=
ENST00000697160.1:c.956-15589T= ENSP00000513149.1:n.956-15589T=
ENST00000697161.1:c.651T= ENSP00000513150.1:n.651T=
ENST00000697162.1:c.1044T= ENSP00000513151.1:n.1044T=
ENST00000697163.1:c.1115T= ENSP00000513152.1:p.Leu372=
ENST00000697164.1:c.1025T= ENSP00000513153.1:p.Leu342=
ENST00000697165.1:c.812T= ENSP00000513154.1:p.Leu271=
ENST00000697223.1:c.864T= ENSP00000513190.1:n.864T=
ENST00000697224.1:c.884+3446T= ENSP00000513191.1:n.884+3446T=
ENST00000697225.1:c.718T= ENSP00000513192.1:n.718T=
ENST00000697226.1:c.738+3446T= ENSP00000513193.1:n.738+3446T=
ENST00000697227.1:c.951T= ENSP00000513194.1:n.951T=
ENST00000697228.1:c.807T= ENSP00000513195.1:n.807T=
ENST00000697229.1:c.885-15589T= ENSP00000513196.1:n.885-15589T=
ENST00000697230.1:c.1025T= ENSP00000513197.1:p.Leu342=
ENST00000697231.1:c.1020T= ENSP00000513198.1:n.1020T=
ENST00000697232.1:c.1044T= ENSP00000513199.1:n.1044T=
ENST00000347310.10:c.1115T= MANE Select ENSP00000321345.5:p.Leu372=
ENST00000637002.1:c.506T= ENSP00000490340.1:p.Leu169=
ENST00000347310.9:c.1115T= ENSP00000321345.5:p.Leu372=
ENST00000395227.2:c.-58-15589T= ENSP00000378652.2:n.-58-15589T=
ENST00000425614.3:c.350T= ENSP00000387640.2:p.Leu117=
ENST00000473881.2:c.191-15589T= ENSP00000486667.1:n.191-15589T=
NM_144701.2:c.1115T= NP_653302.2:p.Leu372=
XM_005270516.2:c.353T= XP_005270573.1:p.Leu118=
XM_011540789.1:c.1205T= XP_011539091.1:p.Leu402=
XM_011540790.1:c.1115T= XP_011539092.1:p.Leu372=
XM_011540791.1:c.1115T= XP_011539093.1:p.Leu372=
XM_011540790.3:c.1115T= XP_011539092.1:p.Leu372=
XM_011540791.3:c.1115T= XP_011539093.1:p.Leu372=
XR_001736993.1:n.1228+3446T=
NM_144701.3:c.1115T= MANE Select NP_653302.2:p.Leu372=