Canonical Allele Identifier: CA340728627
Gene: IL23R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67258755C>G , CM000663.2:g.67258755C>G GRCh38
NC_000001.10:g.67724438C>G , CM000663.1:g.67724438C>G GRCh37
NC_000001.9:g.67497026C>G NCBI36
NG_011498.1:g.97270C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000697149.1:c.1356C>G ENSP00000513138.1:n.1356C>G
ENST00000697150.1:c.1414C>G ENSP00000513139.1:n.1414C>G
ENST00000697151.1:c.1347C>G ENSP00000513140.1:n.1347C>G
ENST00000697164.1:c.1427C>G ENSP00000513153.1:p.Ser476Cys
ENST00000697165.1:c.1214C>G ENSP00000513154.1:p.Ser405Cys
ENST00000347310.10:c.1517C>G MANE Select ENSP00000321345.5:p.Ser506Cys
ENST00000637002.1:c.908C>G ENSP00000490340.1:p.Ser303Cys
ENST00000347310.9:c.1517C>G ENSP00000321345.5:p.Ser506Cys
ENST00000395227.2:c.311C>G ENSP00000378652.2:p.Ser104Cys
ENST00000425614.3:c.752C>G ENSP00000387640.2:p.Ser251Cys
ENST00000473881.2:c.*343C>G ENSP00000486667.1:n.*343C>G
NM_144701.2:c.1517C>G NP_653302.2:p.Ser506Cys
XM_005270516.2:c.755C>G XP_005270573.1:p.Ser252Cys
XM_011540789.1:c.1607C>G XP_011539091.1:p.Ser536Cys
XM_011540790.1:c.1517C>G XP_011539092.1:p.Ser506Cys
XM_011540791.1:c.1517C>G XP_011539093.1:p.Ser506Cys
XM_011540790.3:c.1517C>G XP_011539092.1:p.Ser506Cys
XM_011540791.3:c.1517C>G XP_011539093.1:p.Ser506Cys
XR_001736993.1:n.1597C>G
NM_144701.3:c.1517C>G MANE Select NP_653302.2:p.Ser506Cys