Canonical Allele Identifier: CA900055
Community Standard Title: NM_144701.3(IL23R):c.1790G>C (p.Cys597Ser)
Gene: IL23R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67259028G>C , CM000663.2:g.67259028G>C GRCh38
NC_000001.10:g.67724711G>C , CM000663.1:g.67724711G>C GRCh37
NC_000001.9:g.67497299G>C NCBI36
NG_011498.1:g.97543G>C

Transcript Alleles

HGVS Amino-acid Change
NM_144701.3:c.1790G>C MANE Select NP_653302.2:p.Cys597Ser
ENST00000347310.10:c.1790G>C MANE Select ENSP00000321345.5:p.Cys597Ser
NM_144701.2:c.1790G>C NP_653302.2:p.Cys597Ser
ENST00000347310.9:c.1790G>C ENSP00000321345.5:p.Cys597Ser
ENST00000395227.2:c.584G>C ENSP00000378652.2:p.Cys195Ser
ENST00000425614.3:c.1025G>C ENSP00000387640.2:p.Cys342Ser
ENST00000473881.2:c.*616G>C ENSP00000486667.1:n.*616G>C
ENST00000637002.1:c.1181G>C ENSP00000490340.1:p.Cys394Ser
ENST00000697149.1:c.1629G>C ENSP00000513138.1:n.1629G>C
ENST00000697150.1:c.1687G>C ENSP00000513139.1:n.1687G>C
ENST00000697151.1:c.1620G>C ENSP00000513140.1:n.1620G>C
ENST00000697164.1:c.1700G>C ENSP00000513153.1:p.Cys567Ser
ENST00000697165.1:c.1487G>C ENSP00000513154.1:p.Cys496Ser
XM_005270516.2:c.1028G>C XP_005270573.1:p.Cys343Ser
XM_011540789.1:c.1880G>C XP_011539091.1:p.Cys627Ser
XM_011540790.1:c.1790G>C XP_011539092.1:p.Cys597Ser
XM_011540790.3:c.1790G>C XP_011539092.1:p.Cys597Ser
XM_011540791.1:c.1790G>C XP_011539093.1:p.Cys597Ser
XM_011540791.3:c.1790G>C XP_011539093.1:p.Cys597Ser
XR_001736993.1:n.1870G>C