Canonical Allele Identifier: CA2646123587
Gene: IL23R HGNC NCBI
C1orf141 HGNC NCBI

Linked Data

gnomAD v4: 1-67168116-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67168116C>T , CM000663.2:g.67168116C>T GRCh38
NC_000001.10:g.67633799C>T , CM000663.1:g.67633799C>T GRCh37
NC_000001.9:g.67406387C>T NCBI36
NG_011498.1:g.6631C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000697222.1:c.-5C>T (IL23R) ENSP00000513189.1:n.-5C>T
ENST00000347310.10:c.-5C>T (IL23R) MANE Select ENSP00000321345.5:n.-5C>T
ENST00000637002.1:c.-609C>T (IL23R) ENSP00000490340.1:n.-609C>T
ENST00000347310.9:c.-5C>T (IL23R) ENSP00000321345.5:n.-5C>T
ENST00000371007.6:c.-103-36889G>A (C1orf141) ENSP00000360046.1:n.-103-36889G>A
ENST00000448166.6:c.-103-36889G>A (C1orf141) ENSP00000415519.2:n.-103-36889G>A
NM_144701.2:c.-5C>T (IL23R) NP_653302.2:n.-5C>T
XM_011540789.1:c.86C>T (IL23R) XP_011539091.1:p.Pro29Leu
XM_011540790.1:c.-5C>T (IL23R) XP_011539092.1:n.-5C>T
XM_011540791.1:c.-5C>T (IL23R) XP_011539093.1:n.-5C>T
XM_011540790.3:c.-5C>T (IL23R) XP_011539092.1:n.-5C>T
XM_011540791.3:c.-5C>T (IL23R) XP_011539093.1:n.-5C>T
XR_001736993.1:n.179C>T (IL23R)
NM_144701.3:c.-5C>T (IL23R) MANE Select NP_653302.2:n.-5C>T