Canonical Allele Identifier: CA340729590
Gene: IL23R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67259015G>T , CM000663.2:g.67259015G>T GRCh38
NC_000001.10:g.67724698G>T , CM000663.1:g.67724698G>T GRCh37
NC_000001.9:g.67497286G>T NCBI36
NG_011498.1:g.97530G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000697149.1:c.1616G>T ENSP00000513138.1:n.1616G>T
ENST00000697150.1:c.1674G>T ENSP00000513139.1:n.1674G>T
ENST00000697151.1:c.1607G>T ENSP00000513140.1:n.1607G>T
ENST00000697164.1:c.1687G>T ENSP00000513153.1:p.Glu563Ter
ENST00000697165.1:c.1474G>T ENSP00000513154.1:p.Glu492Ter
ENST00000347310.10:c.1777G>T MANE Select ENSP00000321345.5:p.Glu593Ter
ENST00000637002.1:c.1168G>T ENSP00000490340.1:p.Glu390Ter
ENST00000347310.9:c.1777G>T ENSP00000321345.5:p.Glu593Ter
ENST00000395227.2:c.571G>T ENSP00000378652.2:p.Glu191Ter
ENST00000425614.3:c.1012G>T ENSP00000387640.2:p.Glu338Ter
ENST00000473881.2:c.*603G>T ENSP00000486667.1:n.*603G>T
NM_144701.2:c.1777G>T NP_653302.2:p.Glu593Ter
XM_005270516.2:c.1015G>T XP_005270573.1:p.Glu339Ter
XM_011540789.1:c.1867G>T XP_011539091.1:p.Glu623Ter
XM_011540790.1:c.1777G>T XP_011539092.1:p.Glu593Ter
XM_011540791.1:c.1777G>T XP_011539093.1:p.Glu593Ter
XM_011540790.3:c.1777G>T XP_011539092.1:p.Glu593Ter
XM_011540791.3:c.1777G>T XP_011539093.1:p.Glu593Ter
XR_001736993.1:n.1857G>T
NM_144701.3:c.1777G>T MANE Select NP_653302.2:p.Glu593Ter