Canonical Allele Identifier: CA340728647
Gene: IL23R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67258764T>C , CM000663.2:g.67258764T>C GRCh38
NC_000001.10:g.67724447T>C , CM000663.1:g.67724447T>C GRCh37
NC_000001.9:g.67497035T>C NCBI36
NG_011498.1:g.97279T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000697149.1:c.1365T>C ENSP00000513138.1:n.1365T>C
ENST00000697150.1:c.1423T>C ENSP00000513139.1:n.1423T>C
ENST00000697151.1:c.1356T>C ENSP00000513140.1:n.1356T>C
ENST00000697164.1:c.1436T>C ENSP00000513153.1:p.Leu479Pro
ENST00000697165.1:c.1223T>C ENSP00000513154.1:p.Leu408Pro
ENST00000347310.10:c.1526T>C MANE Select ENSP00000321345.5:p.Leu509Pro
ENST00000637002.1:c.917T>C ENSP00000490340.1:p.Leu306Pro
ENST00000347310.9:c.1526T>C ENSP00000321345.5:p.Leu509Pro
ENST00000395227.2:c.320T>C ENSP00000378652.2:p.Leu107Pro
ENST00000425614.3:c.761T>C ENSP00000387640.2:p.Leu254Pro
ENST00000473881.2:c.*352T>C ENSP00000486667.1:n.*352T>C
NM_144701.2:c.1526T>C NP_653302.2:p.Leu509Pro
XM_005270516.2:c.764T>C XP_005270573.1:p.Leu255Pro
XM_011540789.1:c.1616T>C XP_011539091.1:p.Leu539Pro
XM_011540790.1:c.1526T>C XP_011539092.1:p.Leu509Pro
XM_011540791.1:c.1526T>C XP_011539093.1:p.Leu509Pro
XM_011540790.3:c.1526T>C XP_011539092.1:p.Leu509Pro
XM_011540791.3:c.1526T>C XP_011539093.1:p.Leu509Pro
XR_001736993.1:n.1606T>C
NM_144701.3:c.1526T>C MANE Select NP_653302.2:p.Leu509Pro