Canonical Allele Identifier: CA340725725
Gene: IL23R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67240178G>A , CM000663.2:g.67240178G>A GRCh38
NC_000001.10:g.67705861G>A , CM000663.1:g.67705861G>A GRCh37
NC_000001.9:g.67478449G>A NCBI36
NG_011498.1:g.78693G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000697148.1:c.922-1G>A ENSP00000513137.1:n.922-1G>A
ENST00000697149.1:c.885-1G>A ENSP00000513138.1:n.885-1G>A
ENST00000697150.1:c.1045+3376G>A ENSP00000513139.1:n.1045+3376G>A
ENST00000697151.1:c.1045+3376G>A ENSP00000513140.1:n.1045+3376G>A
ENST00000697152.1:c.799-15659G>A ENSP00000513141.1:n.799-15659G>A
ENST00000697153.1:c.795-15659G>A ENSP00000513142.1:n.795-15659G>A
ENST00000697154.1:c.956-18300G>A ENSP00000513143.1:n.956-18300G>A
ENST00000697155.1:c.649-18300G>A ENSP00000513144.1:n.649-18300G>A
ENST00000697156.1:c.1046-1G>A ENSP00000513145.1:n.1046-1G>A
ENST00000697157.1:c.900-1G>A ENSP00000513146.1:n.900-1G>A
ENST00000697158.1:c.889-1G>A ENSP00000513147.1:n.889-1G>A
ENST00000697159.1:c.739-1G>A ENSP00000513148.1:n.739-1G>A
ENST00000697160.1:c.956-15659G>A ENSP00000513149.1:n.956-15659G>A
ENST00000697161.1:c.582-1G>A ENSP00000513150.1:n.582-1G>A
ENST00000697162.1:c.975-1G>A ENSP00000513151.1:n.975-1G>A
ENST00000697163.1:c.1046-1G>A ENSP00000513152.1:n.1046-1G>A
ENST00000697164.1:c.956-1G>A ENSP00000513153.1:n.956-1G>A
ENST00000697165.1:c.743-1G>A ENSP00000513154.1:n.743-1G>A
ENST00000697223.1:c.795-1G>A ENSP00000513190.1:n.795-1G>A
ENST00000697224.1:c.884+3376G>A ENSP00000513191.1:n.884+3376G>A
ENST00000697225.1:c.649-1G>A ENSP00000513192.1:n.649-1G>A
ENST00000697226.1:c.738+3376G>A ENSP00000513193.1:n.738+3376G>A
ENST00000697227.1:c.882-1G>A ENSP00000513194.1:n.882-1G>A
ENST00000697228.1:c.738-1G>A ENSP00000513195.1:n.738-1G>A
ENST00000697229.1:c.885-15659G>A ENSP00000513196.1:n.885-15659G>A
ENST00000697230.1:c.956-1G>A ENSP00000513197.1:n.956-1G>A
ENST00000697231.1:c.951-1G>A ENSP00000513198.1:n.951-1G>A
ENST00000697232.1:c.975-1G>A ENSP00000513199.1:n.975-1G>A
ENST00000347310.10:c.1046-1G>A MANE Select ENSP00000321345.5:n.1046-1G>A
ENST00000637002.1:c.437-1G>A ENSP00000490340.1:n.437-1G>A
ENST00000347310.9:c.1046-1G>A ENSP00000321345.5:n.1046-1G>A
ENST00000395227.2:c.-58-15659G>A ENSP00000378652.2:n.-58-15659G>A
ENST00000425614.3:c.281-1G>A ENSP00000387640.2:n.281-1G>A
ENST00000473881.2:c.191-15659G>A ENSP00000486667.1:n.191-15659G>A
NM_144701.2:c.1046-1G>A NP_653302.2:n.1046-1G>A
XM_005270516.2:c.284-1G>A XP_005270573.1:n.284-1G>A
XM_011540789.1:c.1136-1G>A XP_011539091.1:n.1136-1G>A
XM_011540790.1:c.1046-1G>A XP_011539092.1:n.1046-1G>A
XM_011540791.1:c.1046-1G>A XP_011539093.1:n.1046-1G>A
XM_011540790.3:c.1046-1G>A XP_011539092.1:n.1046-1G>A
XM_011540791.3:c.1046-1G>A XP_011539093.1:n.1046-1G>A
XR_001736993.1:n.1228+3376G>A
NM_144701.3:c.1046-1G>A MANE Select NP_653302.2:n.1046-1G>A