Canonical Allele Identifier: CA340728827
Gene: IL23R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67258844A>T , CM000663.2:g.67258844A>T GRCh38
NC_000001.10:g.67724527A>T , CM000663.1:g.67724527A>T GRCh37
NC_000001.9:g.67497115A>T NCBI36
NG_011498.1:g.97359A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000697149.1:c.1445A>T ENSP00000513138.1:n.1445A>T
ENST00000697150.1:c.1503A>T ENSP00000513139.1:n.1503A>T
ENST00000697151.1:c.1436A>T ENSP00000513140.1:n.1436A>T
ENST00000697164.1:c.1516A>T ENSP00000513153.1:p.Ser506Cys
ENST00000697165.1:c.1303A>T ENSP00000513154.1:p.Ser435Cys
ENST00000347310.10:c.1606A>T MANE Select ENSP00000321345.5:p.Ser536Cys
ENST00000637002.1:c.997A>T ENSP00000490340.1:p.Ser333Cys
ENST00000347310.9:c.1606A>T ENSP00000321345.5:p.Ser536Cys
ENST00000395227.2:c.400A>T ENSP00000378652.2:p.Ser134Cys
ENST00000425614.3:c.841A>T ENSP00000387640.2:p.Ser281Cys
ENST00000473881.2:c.*432A>T ENSP00000486667.1:n.*432A>T
NM_144701.2:c.1606A>T NP_653302.2:p.Ser536Cys
XM_005270516.2:c.844A>T XP_005270573.1:p.Ser282Cys
XM_011540789.1:c.1696A>T XP_011539091.1:p.Ser566Cys
XM_011540790.1:c.1606A>T XP_011539092.1:p.Ser536Cys
XM_011540791.1:c.1606A>T XP_011539093.1:p.Ser536Cys
XM_011540790.3:c.1606A>T XP_011539092.1:p.Ser536Cys
XM_011540791.3:c.1606A>T XP_011539093.1:p.Ser536Cys
XR_001736993.1:n.1686A>T
NM_144701.3:c.1606A>T MANE Select NP_653302.2:p.Ser536Cys