Canonical Allele Identifier: CA340728609
Gene: IL23R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67258746A>T , CM000663.2:g.67258746A>T GRCh38
NC_000001.10:g.67724429A>T , CM000663.1:g.67724429A>T GRCh37
NC_000001.9:g.67497017A>T NCBI36
NG_011498.1:g.97261A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000697149.1:c.1347A>T ENSP00000513138.1:n.1347A>T
ENST00000697150.1:c.1405A>T ENSP00000513139.1:n.1405A>T
ENST00000697151.1:c.1338A>T ENSP00000513140.1:n.1338A>T
ENST00000697164.1:c.1418A>T ENSP00000513153.1:p.Glu473Val
ENST00000697165.1:c.1205A>T ENSP00000513154.1:p.Glu402Val
ENST00000347310.10:c.1508A>T MANE Select ENSP00000321345.5:p.Glu503Val
ENST00000637002.1:c.899A>T ENSP00000490340.1:p.Glu300Val
ENST00000347310.9:c.1508A>T ENSP00000321345.5:p.Glu503Val
ENST00000395227.2:c.302A>T ENSP00000378652.2:p.Glu101Val
ENST00000425614.3:c.743A>T ENSP00000387640.2:p.Glu248Val
ENST00000473881.2:c.*334A>T ENSP00000486667.1:n.*334A>T
NM_144701.2:c.1508A>T NP_653302.2:p.Glu503Val
XM_005270516.2:c.746A>T XP_005270573.1:p.Glu249Val
XM_011540789.1:c.1598A>T XP_011539091.1:p.Glu533Val
XM_011540790.1:c.1508A>T XP_011539092.1:p.Glu503Val
XM_011540791.1:c.1508A>T XP_011539093.1:p.Glu503Val
XM_011540790.3:c.1508A>T XP_011539092.1:p.Glu503Val
XM_011540791.3:c.1508A>T XP_011539093.1:p.Glu503Val
XR_001736993.1:n.1588A>T
NM_144701.3:c.1508A>T MANE Select NP_653302.2:p.Glu503Val