Canonical Allele Identifier: CA340728788
Gene: IL23R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67258828T>A , CM000663.2:g.67258828T>A GRCh38
NC_000001.10:g.67724511T>A , CM000663.1:g.67724511T>A GRCh37
NC_000001.9:g.67497099T>A NCBI36
NG_011498.1:g.97343T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000697149.1:c.1429T>A ENSP00000513138.1:n.1429T>A
ENST00000697150.1:c.1487T>A ENSP00000513139.1:n.1487T>A
ENST00000697151.1:c.1420T>A ENSP00000513140.1:n.1420T>A
ENST00000697164.1:c.1500T>A ENSP00000513153.1:p.Phe500Leu
ENST00000697165.1:c.1287T>A ENSP00000513154.1:p.Phe429Leu
ENST00000347310.10:c.1590T>A MANE Select ENSP00000321345.5:p.Phe530Leu
ENST00000637002.1:c.981T>A ENSP00000490340.1:p.Phe327Leu
ENST00000347310.9:c.1590T>A ENSP00000321345.5:p.Phe530Leu
ENST00000395227.2:c.384T>A ENSP00000378652.2:p.Phe128Leu
ENST00000425614.3:c.825T>A ENSP00000387640.2:p.Phe275Leu
ENST00000473881.2:c.*416T>A ENSP00000486667.1:n.*416T>A
NM_144701.2:c.1590T>A NP_653302.2:p.Phe530Leu
XM_005270516.2:c.828T>A XP_005270573.1:p.Phe276Leu
XM_011540789.1:c.1680T>A XP_011539091.1:p.Phe560Leu
XM_011540790.1:c.1590T>A XP_011539092.1:p.Phe530Leu
XM_011540791.1:c.1590T>A XP_011539093.1:p.Phe530Leu
XM_011540790.3:c.1590T>A XP_011539092.1:p.Phe530Leu
XM_011540791.3:c.1590T>A XP_011539093.1:p.Phe530Leu
XR_001736993.1:n.1670T>A
NM_144701.3:c.1590T>A MANE Select NP_653302.2:p.Phe530Leu