Canonical Allele Identifier: CA10840333
Gene: IL23R HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10489629

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67222666T>C , CM000663.2:g.67222666T>C GRCh38
NC_000001.10:g.67688349T>C , CM000663.1:g.67688349T>C GRCh37
NC_000001.9:g.67460937T>C NCBI36
NG_011498.1:g.61181T>C

Transcript Alleles

HGVS Amino-acid change
NM_144701.2:c.955+2936T>C VV NP_653302.2:p.=
XM_005270516.2:c.193+2936T>C XP_005270573.1:p.=
XM_011540789.1:c.1045+2936T>C XP_011539091.1:p.=
XM_011540790.1:c.955+2936T>C XP_011539092.1:p.=
XM_011540791.1:c.955+2936T>C XP_011539093.1:p.=
XM_011540790.3:c.955+2936T>C XP_011539092.1:p.=
XM_011540791.3:c.955+2936T>C XP_011539093.1:p.=
XR_001736993.1:n.1138+2936T>C
ENST00000347310.9:c.955+2936T>C ENSP00000321345.5:p.=
ENST00000371007.6:c.-104+9180A>G ENSP00000360046.1:p.=
ENST00000395227.2:c.-59+2936T>C ENSP00000378652.2:p.=
ENST00000425614.3:c.190+2936T>C ENSP00000387640.2:p.=
ENST00000448166.6:c.-104+9180A>G ENSP00000415519.2:p.=
ENST00000473881.2:c.190+2936T>C ENSP00000486667.1:p.=