Canonical Allele Identifier: CA340729079
Gene: IL23R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67258890T>G , CM000663.2:g.67258890T>G GRCh38
NC_000001.10:g.67724573T>G , CM000663.1:g.67724573T>G GRCh37
NC_000001.9:g.67497161T>G NCBI36
NG_011498.1:g.97405T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000697149.1:c.1491T>G ENSP00000513138.1:n.1491T>G
ENST00000697150.1:c.1549T>G ENSP00000513139.1:n.1549T>G
ENST00000697151.1:c.1482T>G ENSP00000513140.1:n.1482T>G
ENST00000697164.1:c.1562T>G ENSP00000513153.1:p.Leu521Arg
ENST00000697165.1:c.1349T>G ENSP00000513154.1:p.Leu450Arg
ENST00000347310.10:c.1652T>G MANE Select ENSP00000321345.5:p.Leu551Arg
ENST00000637002.1:c.1043T>G ENSP00000490340.1:p.Leu348Arg
ENST00000347310.9:c.1652T>G ENSP00000321345.5:p.Leu551Arg
ENST00000395227.2:c.446T>G ENSP00000378652.2:p.Leu149Arg
ENST00000425614.3:c.887T>G ENSP00000387640.2:p.Leu296Arg
ENST00000473881.2:c.*478T>G ENSP00000486667.1:n.*478T>G
NM_144701.2:c.1652T>G NP_653302.2:p.Leu551Arg
XM_005270516.2:c.890T>G XP_005270573.1:p.Leu297Arg
XM_011540789.1:c.1742T>G XP_011539091.1:p.Leu581Arg
XM_011540790.1:c.1652T>G XP_011539092.1:p.Leu551Arg
XM_011540791.1:c.1652T>G XP_011539093.1:p.Leu551Arg
XM_011540790.3:c.1652T>G XP_011539092.1:p.Leu551Arg
XM_011540791.3:c.1652T>G XP_011539093.1:p.Leu551Arg
XR_001736993.1:n.1732T>G
NM_144701.3:c.1652T>G MANE Select NP_653302.2:p.Leu551Arg