Canonical Allele Identifier: CA340725942
Gene: IL23R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67240277A>T , CM000663.2:g.67240277A>T GRCh38
NC_000001.10:g.67705960A>T , CM000663.1:g.67705960A>T GRCh37
NC_000001.9:g.67478548A>T NCBI36
NG_011498.1:g.78792A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000697148.1:c.1020A>T ENSP00000513137.1:n.1020A>T
ENST00000697149.1:c.983A>T ENSP00000513138.1:n.983A>T
ENST00000697150.1:c.1045+3475A>T ENSP00000513139.1:n.1045+3475A>T
ENST00000697151.1:c.1045+3475A>T ENSP00000513140.1:n.1045+3475A>T
ENST00000697152.1:c.799-15560A>T ENSP00000513141.1:n.799-15560A>T
ENST00000697153.1:c.795-15560A>T ENSP00000513142.1:n.795-15560A>T
ENST00000697154.1:c.956-18201A>T ENSP00000513143.1:n.956-18201A>T
ENST00000697155.1:c.649-18201A>T ENSP00000513144.1:n.649-18201A>T
ENST00000697156.1:c.1144A>T ENSP00000513145.1:p.Thr382Ser
ENST00000697157.1:c.998A>T ENSP00000513146.1:n.998A>T
ENST00000697158.1:c.987A>T ENSP00000513147.1:n.987A>T
ENST00000697159.1:c.837A>T ENSP00000513148.1:n.837A>T
ENST00000697160.1:c.956-15560A>T ENSP00000513149.1:n.956-15560A>T
ENST00000697161.1:c.680A>T ENSP00000513150.1:n.680A>T
ENST00000697162.1:c.1073A>T ENSP00000513151.1:n.1073A>T
ENST00000697163.1:c.1144A>T ENSP00000513152.1:p.Thr382Ser
ENST00000697164.1:c.1054A>T ENSP00000513153.1:p.Thr352Ser
ENST00000697165.1:c.841A>T ENSP00000513154.1:p.Thr281Ser
ENST00000697223.1:c.893A>T ENSP00000513190.1:n.893A>T
ENST00000697224.1:c.884+3475A>T ENSP00000513191.1:n.884+3475A>T
ENST00000697225.1:c.747A>T ENSP00000513192.1:n.747A>T
ENST00000697226.1:c.738+3475A>T ENSP00000513193.1:n.738+3475A>T
ENST00000697227.1:c.980A>T ENSP00000513194.1:n.980A>T
ENST00000697228.1:c.836A>T ENSP00000513195.1:n.836A>T
ENST00000697229.1:c.885-15560A>T ENSP00000513196.1:n.885-15560A>T
ENST00000697230.1:c.1054A>T ENSP00000513197.1:p.Thr352Ser
ENST00000697231.1:c.1049A>T ENSP00000513198.1:n.1049A>T
ENST00000697232.1:c.1073A>T ENSP00000513199.1:n.1073A>T
ENST00000347310.10:c.1144A>T MANE Select ENSP00000321345.5:p.Thr382Ser
ENST00000637002.1:c.535A>T ENSP00000490340.1:p.Thr179Ser
ENST00000347310.9:c.1144A>T ENSP00000321345.5:p.Thr382Ser
ENST00000395227.2:c.-58-15560A>T ENSP00000378652.2:n.-58-15560A>T
ENST00000425614.3:c.379A>T ENSP00000387640.2:p.Thr127Ser
ENST00000473881.2:c.191-15560A>T ENSP00000486667.1:n.191-15560A>T
NM_144701.2:c.1144A>T NP_653302.2:p.Thr382Ser
XM_005270516.2:c.382A>T XP_005270573.1:p.Thr128Ser
XM_011540789.1:c.1234A>T XP_011539091.1:p.Thr412Ser
XM_011540790.1:c.1144A>T XP_011539092.1:p.Thr382Ser
XM_011540791.1:c.1144A>T XP_011539093.1:p.Thr382Ser
XM_011540790.3:c.1144A>T XP_011539092.1:p.Thr382Ser
XM_011540791.3:c.1144A>T XP_011539093.1:p.Thr382Ser
XR_001736993.1:n.1228+3475A>T
NM_144701.3:c.1144A>T MANE Select NP_653302.2:p.Thr382Ser