Canonical Allele Identifier: CA340728732
Gene: IL23R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67258805A>G , CM000663.2:g.67258805A>G GRCh38
NC_000001.10:g.67724488A>G , CM000663.1:g.67724488A>G GRCh37
NC_000001.9:g.67497076A>G NCBI36
NG_011498.1:g.97320A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000697149.1:c.1406A>G ENSP00000513138.1:n.1406A>G
ENST00000697150.1:c.1464A>G ENSP00000513139.1:n.1464A>G
ENST00000697151.1:c.1397A>G ENSP00000513140.1:n.1397A>G
ENST00000697164.1:c.1477A>G ENSP00000513153.1:p.Arg493Gly
ENST00000697165.1:c.1264A>G ENSP00000513154.1:p.Arg422Gly
ENST00000347310.10:c.1567A>G MANE Select ENSP00000321345.5:p.Arg523Gly
ENST00000637002.1:c.958A>G ENSP00000490340.1:p.Arg320Gly
ENST00000347310.9:c.1567A>G ENSP00000321345.5:p.Arg523Gly
ENST00000395227.2:c.361A>G ENSP00000378652.2:p.Arg121Gly
ENST00000425614.3:c.802A>G ENSP00000387640.2:p.Arg268Gly
ENST00000473881.2:c.*393A>G ENSP00000486667.1:n.*393A>G
NM_144701.2:c.1567A>G NP_653302.2:p.Arg523Gly
XM_005270516.2:c.805A>G XP_005270573.1:p.Arg269Gly
XM_011540789.1:c.1657A>G XP_011539091.1:p.Arg553Gly
XM_011540790.1:c.1567A>G XP_011539092.1:p.Arg523Gly
XM_011540791.1:c.1567A>G XP_011539093.1:p.Arg523Gly
XM_011540790.3:c.1567A>G XP_011539092.1:p.Arg523Gly
XM_011540791.3:c.1567A>G XP_011539093.1:p.Arg523Gly
XR_001736993.1:n.1647A>G
NM_144701.3:c.1567A>G MANE Select NP_653302.2:p.Arg523Gly