Canonical Allele Identifier: CA340728921
Gene: IL23R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67258866C>T , CM000663.2:g.67258866C>T GRCh38
NC_000001.10:g.67724549C>T , CM000663.1:g.67724549C>T GRCh37
NC_000001.9:g.67497137C>T NCBI36
NG_011498.1:g.97381C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000697149.1:c.1467C>T ENSP00000513138.1:n.1467C>T
ENST00000697150.1:c.1525C>T ENSP00000513139.1:n.1525C>T
ENST00000697151.1:c.1458C>T ENSP00000513140.1:n.1458C>T
ENST00000697164.1:c.1538C>T ENSP00000513153.1:p.Thr513Ile
ENST00000697165.1:c.1325C>T ENSP00000513154.1:p.Thr442Ile
ENST00000347310.10:c.1628C>T MANE Select ENSP00000321345.5:p.Thr543Ile
ENST00000637002.1:c.1019C>T ENSP00000490340.1:p.Thr340Ile
ENST00000347310.9:c.1628C>T ENSP00000321345.5:p.Thr543Ile
ENST00000395227.2:c.422C>T ENSP00000378652.2:p.Thr141Ile
ENST00000425614.3:c.863C>T ENSP00000387640.2:p.Thr288Ile
ENST00000473881.2:c.*454C>T ENSP00000486667.1:n.*454C>T
NM_144701.2:c.1628C>T NP_653302.2:p.Thr543Ile
XM_005270516.2:c.866C>T XP_005270573.1:p.Thr289Ile
XM_011540789.1:c.1718C>T XP_011539091.1:p.Thr573Ile
XM_011540790.1:c.1628C>T XP_011539092.1:p.Thr543Ile
XM_011540791.1:c.1628C>T XP_011539093.1:p.Thr543Ile
XM_011540790.3:c.1628C>T XP_011539092.1:p.Thr543Ile
XM_011540791.3:c.1628C>T XP_011539093.1:p.Thr543Ile
XR_001736993.1:n.1708C>T
NM_144701.3:c.1628C>T MANE Select NP_653302.2:p.Thr543Ile