Canonical Allele Identifier: CA1173025867
Gene: IL23R HGNC NCBI
C1orf141 HGNC NCBI

Linked Data

dbSNP Id: rs1646895080

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67168078T>A , CM000663.2:g.67168078T>A GRCh38
NC_000001.10:g.67633761T>A , CM000663.1:g.67633761T>A GRCh37
NC_000001.9:g.67406349T>A NCBI36
NG_011498.1:g.6593T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000697222.1:c.-29-14T>A (IL23R) ENSP00000513189.1:n.-29-14T>A
ENST00000347310.10:c.-29-14T>A (IL23R) MANE Select ENSP00000321345.5:n.-29-14T>A
ENST00000637002.1:c.-633-14T>A (IL23R) ENSP00000490340.1:n.-633-14T>A
ENST00000347310.9:c.-29-14T>A (IL23R) ENSP00000321345.5:n.-29-14T>A
ENST00000371007.6:c.-103-36851A>T (C1orf141) ENSP00000360046.1:n.-103-36851A>T
ENST00000448166.6:c.-103-36851A>T (C1orf141) ENSP00000415519.2:n.-103-36851A>T
NM_144701.2:c.-29-14T>A (IL23R) NP_653302.2:n.-29-14T>A
XM_011540789.1:c.62-14T>A (IL23R) XP_011539091.1:n.62-14T>A
XM_011540790.1:c.-29-14T>A (IL23R) XP_011539092.1:n.-29-14T>A
XM_011540791.1:c.-29-14T>A (IL23R) XP_011539093.1:n.-29-14T>A
XM_011540790.3:c.-29-14T>A (IL23R) XP_011539092.1:n.-29-14T>A
XM_011540791.3:c.-29-14T>A (IL23R) XP_011539093.1:n.-29-14T>A
XR_001736993.1:n.155-14T>A (IL23R)
NM_144701.3:c.-29-14T>A (IL23R) MANE Select NP_653302.2:n.-29-14T>A