Canonical Allele Identifier: CA1173056546
Gene: IL23R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67240234G= , CM000663.2:g.67240234G= GRCh38
NC_000001.10:g.67705917G= , CM000663.1:g.67705917G= GRCh37
NC_000001.9:g.67478505G= NCBI36
NG_011498.1:g.78749G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697148.1:c.977G= ENSP00000513137.1:n.977G=
ENST00000697149.1:c.940G= ENSP00000513138.1:n.940G=
ENST00000697150.1:c.1045+3432G= ENSP00000513139.1:n.1045+3432G=
ENST00000697151.1:c.1045+3432G= ENSP00000513140.1:n.1045+3432G=
ENST00000697152.1:c.799-15603G= ENSP00000513141.1:n.799-15603G=
ENST00000697153.1:c.795-15603G= ENSP00000513142.1:n.795-15603G=
ENST00000697154.1:c.956-18244G= ENSP00000513143.1:n.956-18244G=
ENST00000697155.1:c.649-18244G= ENSP00000513144.1:n.649-18244G=
ENST00000697156.1:c.1101G= ENSP00000513145.1:p.Leu367=
ENST00000697157.1:c.955G= ENSP00000513146.1:n.955G=
ENST00000697158.1:c.944G= ENSP00000513147.1:n.944G=
ENST00000697159.1:c.794G= ENSP00000513148.1:n.794G=
ENST00000697160.1:c.956-15603G= ENSP00000513149.1:n.956-15603G=
ENST00000697161.1:c.637G= ENSP00000513150.1:n.637G=
ENST00000697162.1:c.1030G= ENSP00000513151.1:n.1030G=
ENST00000697163.1:c.1101G= ENSP00000513152.1:p.Leu367=
ENST00000697164.1:c.1011G= ENSP00000513153.1:p.Leu337=
ENST00000697165.1:c.798G= ENSP00000513154.1:p.Leu266=
ENST00000697223.1:c.850G= ENSP00000513190.1:n.850G=
ENST00000697224.1:c.884+3432G= ENSP00000513191.1:n.884+3432G=
ENST00000697225.1:c.704G= ENSP00000513192.1:n.704G=
ENST00000697226.1:c.738+3432G= ENSP00000513193.1:n.738+3432G=
ENST00000697227.1:c.937G= ENSP00000513194.1:n.937G=
ENST00000697228.1:c.793G= ENSP00000513195.1:n.793G=
ENST00000697229.1:c.885-15603G= ENSP00000513196.1:n.885-15603G=
ENST00000697230.1:c.1011G= ENSP00000513197.1:p.Leu337=
ENST00000697231.1:c.1006G= ENSP00000513198.1:n.1006G=
ENST00000697232.1:c.1030G= ENSP00000513199.1:n.1030G=
ENST00000347310.10:c.1101G= MANE Select ENSP00000321345.5:p.Leu367=
ENST00000637002.1:c.492G= ENSP00000490340.1:p.Leu164=
ENST00000347310.9:c.1101G= ENSP00000321345.5:p.Leu367=
ENST00000395227.2:c.-58-15603G= ENSP00000378652.2:n.-58-15603G=
ENST00000425614.3:c.336G= ENSP00000387640.2:p.Leu112=
ENST00000473881.2:c.191-15603G= ENSP00000486667.1:n.191-15603G=
NM_144701.2:c.1101G= NP_653302.2:p.Leu367=
XM_005270516.2:c.339G= XP_005270573.1:p.Leu113=
XM_011540789.1:c.1191G= XP_011539091.1:p.Leu397=
XM_011540790.1:c.1101G= XP_011539092.1:p.Leu367=
XM_011540791.1:c.1101G= XP_011539093.1:p.Leu367=
XM_011540790.3:c.1101G= XP_011539092.1:p.Leu367=
XM_011540791.3:c.1101G= XP_011539093.1:p.Leu367=
XR_001736993.1:n.1228+3432G=
NM_144701.3:c.1101G= MANE Select NP_653302.2:p.Leu367=