Canonical Allele Identifier: CA1143502839
Gene: IL23R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67240250A= , CM000663.2:g.67240250A= GRCh38
NC_000001.10:g.67705933A= , CM000663.1:g.67705933A= GRCh37
NC_000001.9:g.67478521A= NCBI36
NG_011498.1:g.78765A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697148.1:c.993A= ENSP00000513137.1:n.993A=
ENST00000697149.1:c.956A= ENSP00000513138.1:n.956A=
ENST00000697150.1:c.1045+3448A= ENSP00000513139.1:n.1045+3448A=
ENST00000697151.1:c.1045+3448A= ENSP00000513140.1:n.1045+3448A=
ENST00000697152.1:c.799-15587A= ENSP00000513141.1:n.799-15587A=
ENST00000697153.1:c.795-15587A= ENSP00000513142.1:n.795-15587A=
ENST00000697154.1:c.956-18228A= ENSP00000513143.1:n.956-18228A=
ENST00000697155.1:c.649-18228A= ENSP00000513144.1:n.649-18228A=
ENST00000697156.1:c.1117A= ENSP00000513145.1:p.Ile373=
ENST00000697157.1:c.971A= ENSP00000513146.1:n.971A=
ENST00000697158.1:c.960A= ENSP00000513147.1:n.960A=
ENST00000697159.1:c.810A= ENSP00000513148.1:n.810A=
ENST00000697160.1:c.956-15587A= ENSP00000513149.1:n.956-15587A=
ENST00000697161.1:c.653A= ENSP00000513150.1:n.653A=
ENST00000697162.1:c.1046A= ENSP00000513151.1:n.1046A=
ENST00000697163.1:c.1117A= ENSP00000513152.1:p.Ile373=
ENST00000697164.1:c.1027A= ENSP00000513153.1:p.Ile343=
ENST00000697165.1:c.814A= ENSP00000513154.1:p.Ile272=
ENST00000697223.1:c.866A= ENSP00000513190.1:n.866A=
ENST00000697224.1:c.884+3448A= ENSP00000513191.1:n.884+3448A=
ENST00000697225.1:c.720A= ENSP00000513192.1:n.720A=
ENST00000697226.1:c.738+3448A= ENSP00000513193.1:n.738+3448A=
ENST00000697227.1:c.953A= ENSP00000513194.1:n.953A=
ENST00000697228.1:c.809A= ENSP00000513195.1:n.809A=
ENST00000697229.1:c.885-15587A= ENSP00000513196.1:n.885-15587A=
ENST00000697230.1:c.1027A= ENSP00000513197.1:p.Ile343=
ENST00000697231.1:c.1022A= ENSP00000513198.1:n.1022A=
ENST00000697232.1:c.1046A= ENSP00000513199.1:n.1046A=
ENST00000347310.10:c.1117A= MANE Select ENSP00000321345.5:p.Ile373=
ENST00000637002.1:c.508A= ENSP00000490340.1:p.Ile170=
ENST00000347310.9:c.1117A= ENSP00000321345.5:p.Ile373=
ENST00000395227.2:c.-58-15587A= ENSP00000378652.2:n.-58-15587A=
ENST00000425614.3:c.352A= ENSP00000387640.2:p.Ile118=
ENST00000473881.2:c.191-15587A= ENSP00000486667.1:n.191-15587A=
NM_144701.2:c.1117A= NP_653302.2:p.Ile373=
XM_005270516.2:c.355A= XP_005270573.1:p.Ile119=
XM_011540789.1:c.1207A= XP_011539091.1:p.Ile403=
XM_011540790.1:c.1117A= XP_011539092.1:p.Ile373=
XM_011540791.1:c.1117A= XP_011539093.1:p.Ile373=
XM_011540790.3:c.1117A= XP_011539092.1:p.Ile373=
XM_011540791.3:c.1117A= XP_011539093.1:p.Ile373=
XR_001736993.1:n.1228+3448A=
NM_144701.3:c.1117A= MANE Select NP_653302.2:p.Ile373=