Canonical Allele Identifier: CA1173061657
Gene: IL23R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67255121T= , CM000663.2:g.67255121T= GRCh38
NC_000001.10:g.67720804T= , CM000663.1:g.67720804T= GRCh37
NC_000001.9:g.67493392T= NCBI36
NG_011498.1:g.93636T=

Transcript Alleles

HGVS Amino-acid change
ENST00000697148.1:c.1025-716T= ENSP00000513137.1:n.1025-716T=
ENST00000697149.1:c.988-716T= ENSP00000513138.1:n.988-716T=
ENST00000697150.1:c.1046-716T= ENSP00000513139.1:n.1046-716T=
ENST00000697151.1:c.1046-716T= ENSP00000513140.1:n.1046-716T=
ENST00000697152.1:c.799-716T= ENSP00000513141.1:n.799-716T=
ENST00000697153.1:c.795-716T= ENSP00000513142.1:n.795-716T=
ENST00000697154.1:c.956-3357T= ENSP00000513143.1:n.956-3357T=
ENST00000697155.1:c.649-3357T= ENSP00000513144.1:n.649-3357T=
ENST00000697156.1:c.1282-716T= ENSP00000513145.1:n.1282-716T=
ENST00000697157.1:c.1003-716T= ENSP00000513146.1:n.1003-716T=
ENST00000697158.1:c.992-716T= ENSP00000513147.1:n.992-716T=
ENST00000697159.1:c.842-716T= ENSP00000513148.1:n.842-716T=
ENST00000697160.1:c.956-716T= ENSP00000513149.1:n.956-716T=
ENST00000697161.1:c.685-716T= ENSP00000513150.1:n.685-716T=
ENST00000697162.1:c.1078-716T= ENSP00000513151.1:n.1078-716T=
ENST00000697163.1:c.1149-716T= ENSP00000513152.1:n.1149-716T=
ENST00000697164.1:c.1059-716T= ENSP00000513153.1:n.1059-716T=
ENST00000697165.1:c.846-716T= ENSP00000513154.1:n.846-716T=
ENST00000697223.1:c.898-716T= ENSP00000513190.1:n.898-716T=
ENST00000697224.1:c.885-716T= ENSP00000513191.1:n.885-716T=
ENST00000697225.1:c.752-716T= ENSP00000513192.1:n.752-716T=
ENST00000697226.1:c.739-716T= ENSP00000513193.1:n.739-716T=
ENST00000697227.1:c.985-716T= ENSP00000513194.1:n.985-716T=
ENST00000697228.1:c.841-716T= ENSP00000513195.1:n.841-716T=
ENST00000697229.1:c.885-716T= ENSP00000513196.1:n.885-716T=
ENST00000697230.1:c.1059-716T= ENSP00000513197.1:n.1059-716T=
ENST00000697231.1:c.1054-716T= ENSP00000513198.1:n.1054-716T=
ENST00000697232.1:c.1240-716T= ENSP00000513199.1:n.1240-716T=
ENST00000347310.10:c.1149-716T= MANE Select ENSP00000321345.5:n.1149-716T=
ENST00000637002.1:c.540-716T= ENSP00000490340.1:n.540-716T=
ENST00000347310.9:c.1149-716T= ENSP00000321345.5:n.1149-716T=
ENST00000395227.2:c.-58-716T= ENSP00000378652.2:n.-58-716T=
ENST00000425614.3:c.384-716T= ENSP00000387640.2:n.384-716T=
ENST00000473881.2:c.191-716T= ENSP00000486667.1:n.191-716T=
NM_144701.2:c.1149-716T= NP_653302.2:n.1149-716T=
XM_005270516.2:c.387-716T= XP_005270573.1:n.387-716T=
XM_011540789.1:c.1239-716T= XP_011539091.1:n.1239-716T=
XM_011540790.1:c.1149-716T= XP_011539092.1:n.1149-716T=
XM_011540791.1:c.1149-716T= XP_011539093.1:n.1149-716T=
XM_011540790.3:c.1149-716T= XP_011539092.1:n.1149-716T=
XM_011540791.3:c.1149-716T= XP_011539093.1:n.1149-716T=
XR_001736993.1:n.1229-716T=
NM_144701.3:c.1149-716T= MANE Select NP_653302.2:n.1149-716T=