Canonical Allele Identifier: CA1144067589
Gene: IL23R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67240211A= , CM000663.2:g.67240211A= GRCh38
NC_000001.10:g.67705894A= , CM000663.1:g.67705894A= GRCh37
NC_000001.9:g.67478482A= NCBI36
NG_011498.1:g.78726A=

Transcript Alleles

HGVS Amino-acid change
ENST00000697148.1:c.954A= ENSP00000513137.1:n.954A=
ENST00000697149.1:c.917A= ENSP00000513138.1:n.917A=
ENST00000697150.1:c.1045+3409A= ENSP00000513139.1:n.1045+3409A=
ENST00000697151.1:c.1045+3409A= ENSP00000513140.1:n.1045+3409A=
ENST00000697152.1:c.799-15626A= ENSP00000513141.1:n.799-15626A=
ENST00000697153.1:c.795-15626A= ENSP00000513142.1:n.795-15626A=
ENST00000697154.1:c.956-18267A= ENSP00000513143.1:n.956-18267A=
ENST00000697155.1:c.649-18267A= ENSP00000513144.1:n.649-18267A=
ENST00000697156.1:c.1078A= ENSP00000513145.1:p.Met360=
ENST00000697157.1:c.932A= ENSP00000513146.1:n.932A=
ENST00000697158.1:c.921A= ENSP00000513147.1:n.921A=
ENST00000697159.1:c.771A= ENSP00000513148.1:n.771A=
ENST00000697160.1:c.956-15626A= ENSP00000513149.1:n.956-15626A=
ENST00000697161.1:c.614A= ENSP00000513150.1:n.614A=
ENST00000697162.1:c.1007A= ENSP00000513151.1:n.1007A=
ENST00000697163.1:c.1078A= ENSP00000513152.1:p.Met360=
ENST00000697164.1:c.988A= ENSP00000513153.1:p.Met330=
ENST00000697165.1:c.775A= ENSP00000513154.1:p.Met259=
ENST00000697223.1:c.827A= ENSP00000513190.1:n.827A=
ENST00000697224.1:c.884+3409A= ENSP00000513191.1:n.884+3409A=
ENST00000697225.1:c.681A= ENSP00000513192.1:n.681A=
ENST00000697226.1:c.738+3409A= ENSP00000513193.1:n.738+3409A=
ENST00000697227.1:c.914A= ENSP00000513194.1:n.914A=
ENST00000697228.1:c.770A= ENSP00000513195.1:n.770A=
ENST00000697229.1:c.885-15626A= ENSP00000513196.1:n.885-15626A=
ENST00000697230.1:c.988A= ENSP00000513197.1:p.Met330=
ENST00000697231.1:c.983A= ENSP00000513198.1:n.983A=
ENST00000697232.1:c.1007A= ENSP00000513199.1:n.1007A=
ENST00000347310.10:c.1078A= MANE Select ENSP00000321345.5:p.Met360=
ENST00000637002.1:c.469A= ENSP00000490340.1:p.Met157=
ENST00000347310.9:c.1078A= ENSP00000321345.5:p.Met360=
ENST00000395227.2:c.-58-15626A= ENSP00000378652.2:n.-58-15626A=
ENST00000425614.3:c.313A= ENSP00000387640.2:p.Met105=
ENST00000473881.2:c.191-15626A= ENSP00000486667.1:n.191-15626A=
NM_144701.2:c.1078A= NP_653302.2:p.Met360=
XM_005270516.2:c.316A= XP_005270573.1:p.Met106=
XM_011540789.1:c.1168A= XP_011539091.1:p.Met390=
XM_011540790.1:c.1078A= XP_011539092.1:p.Met360=
XM_011540791.1:c.1078A= XP_011539093.1:p.Met360=
XM_011540790.3:c.1078A= XP_011539092.1:p.Met360=
XM_011540791.3:c.1078A= XP_011539093.1:p.Met360=
XR_001736993.1:n.1228+3409A=
NM_144701.3:c.1078A= MANE Select NP_653302.2:p.Met360=