Canonical Allele Identifier: CA340729195

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724597G>C (hg19) ; chr1:g.67258914G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258914G>C , CM000663.2:g.67258914G>C	GRCh38
NC_000001.10:g.67724597G>C , CM000663.1:g.67724597G>C	GRCh37
NC_000001.9:g.67497185G>C	NCBI36
NG_011498.1:g.97429G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1515G>C	ENSP00000513138.1:n.1515G>C
ENST00000697150.1:c.1573G>C	ENSP00000513139.1:n.1573G>C
ENST00000697151.1:c.1506G>C	ENSP00000513140.1:n.1506G>C
ENST00000697164.1:c.1586G>C	ENSP00000513153.1:p.Ser529Thr
ENST00000697165.1:c.1373G>C	ENSP00000513154.1:p.Ser458Thr
ENST00000347310.10:c.1676G>C MANE Select	ENSP00000321345.5:p.Ser559Thr
ENST00000637002.1:c.1067G>C	ENSP00000490340.1:p.Ser356Thr
ENST00000347310.9:c.1676G>C	ENSP00000321345.5:p.Ser559Thr
ENST00000395227.2:c.470G>C	ENSP00000378652.2:p.Ser157Thr
ENST00000425614.3:c.911G>C	ENSP00000387640.2:p.Ser304Thr
ENST00000473881.2:c.*502G>C	ENSP00000486667.1:n.*502G>C
NM_144701.2:c.1676G>C	NP_653302.2:p.Ser559Thr
XM_005270516.2:c.914G>C	XP_005270573.1:p.Ser305Thr
XM_011540789.1:c.1766G>C	XP_011539091.1:p.Ser589Thr
XM_011540790.1:c.1676G>C	XP_011539092.1:p.Ser559Thr
XM_011540791.1:c.1676G>C	XP_011539093.1:p.Ser559Thr
XM_011540790.3:c.1676G>C	XP_011539092.1:p.Ser559Thr
XM_011540791.3:c.1676G>C	XP_011539093.1:p.Ser559Thr
XR_001736993.1:n.1756G>C
NM_144701.3:c.1676G>C MANE Select	NP_653302.2:p.Ser559Thr