Canonical Allele Identifier: CA340728534
Gene: IL23R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67258733A>G , CM000663.2:g.67258733A>G GRCh38
NC_000001.10:g.67724416A>G , CM000663.1:g.67724416A>G GRCh37
NC_000001.9:g.67497004A>G NCBI36
NG_011498.1:g.97248A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000697149.1:c.1334A>G ENSP00000513138.1:n.1334A>G
ENST00000697150.1:c.1392A>G ENSP00000513139.1:n.1392A>G
ENST00000697151.1:c.1325A>G ENSP00000513140.1:n.1325A>G
ENST00000697164.1:c.1405A>G ENSP00000513153.1:p.Ser469Gly
ENST00000697165.1:c.1192A>G ENSP00000513154.1:p.Ser398Gly
ENST00000347310.10:c.1495A>G MANE Select ENSP00000321345.5:p.Ser499Gly
ENST00000637002.1:c.886A>G ENSP00000490340.1:p.Ser296Gly
ENST00000347310.9:c.1495A>G ENSP00000321345.5:p.Ser499Gly
ENST00000395227.2:c.289A>G ENSP00000378652.2:p.Ser97Gly
ENST00000425614.3:c.730A>G ENSP00000387640.2:p.Ser244Gly
ENST00000473881.2:c.*321A>G ENSP00000486667.1:n.*321A>G
NM_144701.2:c.1495A>G NP_653302.2:p.Ser499Gly
XM_005270516.2:c.733A>G XP_005270573.1:p.Ser245Gly
XM_011540789.1:c.1585A>G XP_011539091.1:p.Ser529Gly
XM_011540790.1:c.1495A>G XP_011539092.1:p.Ser499Gly
XM_011540791.1:c.1495A>G XP_011539093.1:p.Ser499Gly
XM_011540790.3:c.1495A>G XP_011539092.1:p.Ser499Gly
XM_011540791.3:c.1495A>G XP_011539093.1:p.Ser499Gly
XR_001736993.1:n.1575A>G
NM_144701.3:c.1495A>G MANE Select NP_653302.2:p.Ser499Gly