Canonical Allele Identifier: CA1173025882
Gene: IL23R HGNC NCBI
C1orf141 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67168114T= , CM000663.2:g.67168114T= GRCh38
NC_000001.10:g.67633797T= , CM000663.1:g.67633797T= GRCh37
NC_000001.9:g.67406385T= NCBI36
NG_011498.1:g.6629T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697222.1:c.-7T= (IL23R) ENSP00000513189.1:n.-7T=
ENST00000347310.10:c.-7T= (IL23R) MANE Select ENSP00000321345.5:n.-7T=
ENST00000637002.1:c.-611T= (IL23R) ENSP00000490340.1:n.-611T=
ENST00000347310.9:c.-7T= (IL23R) ENSP00000321345.5:n.-7T=
ENST00000371007.6:c.-103-36887A= (C1orf141) ENSP00000360046.1:n.-103-36887A=
ENST00000448166.6:c.-103-36887A= (C1orf141) ENSP00000415519.2:n.-103-36887A=
NM_144701.2:c.-7T= (IL23R) NP_653302.2:n.-7T=
XM_011540789.1:c.84T= (IL23R) XP_011539091.1:p.Leu28=
XM_011540790.1:c.-7T= (IL23R) XP_011539092.1:n.-7T=
XM_011540791.1:c.-7T= (IL23R) XP_011539093.1:n.-7T=
XM_011540790.3:c.-7T= (IL23R) XP_011539092.1:n.-7T=
XM_011540791.3:c.-7T= (IL23R) XP_011539093.1:n.-7T=
XR_001736993.1:n.177T= (IL23R)
NM_144701.3:c.-7T= (IL23R) MANE Select NP_653302.2:n.-7T=