Canonical Allele Identifier: CA340728701
Gene: IL23R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67258790T>A , CM000663.2:g.67258790T>A GRCh38
NC_000001.10:g.67724473T>A , CM000663.1:g.67724473T>A GRCh37
NC_000001.9:g.67497061T>A NCBI36
NG_011498.1:g.97305T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000697149.1:c.1391T>A ENSP00000513138.1:n.1391T>A
ENST00000697150.1:c.1449T>A ENSP00000513139.1:n.1449T>A
ENST00000697151.1:c.1382T>A ENSP00000513140.1:n.1382T>A
ENST00000697164.1:c.1462T>A ENSP00000513153.1:p.Ser488Thr
ENST00000697165.1:c.1249T>A ENSP00000513154.1:p.Ser417Thr
ENST00000347310.10:c.1552T>A MANE Select ENSP00000321345.5:p.Ser518Thr
ENST00000637002.1:c.943T>A ENSP00000490340.1:p.Ser315Thr
ENST00000347310.9:c.1552T>A ENSP00000321345.5:p.Ser518Thr
ENST00000395227.2:c.346T>A ENSP00000378652.2:p.Ser116Thr
ENST00000425614.3:c.787T>A ENSP00000387640.2:p.Ser263Thr
ENST00000473881.2:c.*378T>A ENSP00000486667.1:n.*378T>A
NM_144701.2:c.1552T>A NP_653302.2:p.Ser518Thr
XM_005270516.2:c.790T>A XP_005270573.1:p.Ser264Thr
XM_011540789.1:c.1642T>A XP_011539091.1:p.Ser548Thr
XM_011540790.1:c.1552T>A XP_011539092.1:p.Ser518Thr
XM_011540791.1:c.1552T>A XP_011539093.1:p.Ser518Thr
XM_011540790.3:c.1552T>A XP_011539092.1:p.Ser518Thr
XM_011540791.3:c.1552T>A XP_011539093.1:p.Ser518Thr
XR_001736993.1:n.1632T>A
NM_144701.3:c.1552T>A MANE Select NP_653302.2:p.Ser518Thr