Canonical Allele Identifier: CA340728626

Gene: IL23R

Linked Data

• gnomAD v4: 1-67258754-T-C
• MyVariant Identifiers: chr1:g.67724437T>C (hg19) ; chr1:g.67258754T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258754T>C , CM000663.2:g.67258754T>C	GRCh38
NC_000001.10:g.67724437T>C , CM000663.1:g.67724437T>C	GRCh37
NC_000001.9:g.67497025T>C	NCBI36
NG_011498.1:g.97269T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1355T>C	ENSP00000513138.1:n.1355T>C
ENST00000697150.1:c.1413T>C	ENSP00000513139.1:n.1413T>C
ENST00000697151.1:c.1346T>C	ENSP00000513140.1:n.1346T>C
ENST00000697164.1:c.1426T>C	ENSP00000513153.1:p.Ser476Pro
ENST00000697165.1:c.1213T>C	ENSP00000513154.1:p.Ser405Pro
ENST00000347310.10:c.1516T>C MANE Select	ENSP00000321345.5:p.Ser506Pro
ENST00000637002.1:c.907T>C	ENSP00000490340.1:p.Ser303Pro
ENST00000347310.9:c.1516T>C	ENSP00000321345.5:p.Ser506Pro
ENST00000395227.2:c.310T>C	ENSP00000378652.2:p.Ser104Pro
ENST00000425614.3:c.751T>C	ENSP00000387640.2:p.Ser251Pro
ENST00000473881.2:c.*342T>C	ENSP00000486667.1:n.*342T>C
NM_144701.2:c.1516T>C	NP_653302.2:p.Ser506Pro
XM_005270516.2:c.754T>C	XP_005270573.1:p.Ser252Pro
XM_011540789.1:c.1606T>C	XP_011539091.1:p.Ser536Pro
XM_011540790.1:c.1516T>C	XP_011539092.1:p.Ser506Pro
XM_011540791.1:c.1516T>C	XP_011539093.1:p.Ser506Pro
XM_011540790.3:c.1516T>C	XP_011539092.1:p.Ser506Pro
XM_011540791.3:c.1516T>C	XP_011539093.1:p.Ser506Pro
XR_001736993.1:n.1596T>C
NM_144701.3:c.1516T>C MANE Select	NP_653302.2:p.Ser506Pro