Canonical Allele Identifier: CA340729757

Gene: IL23R

Linked Data

• gnomAD v4: 1-67259058-C-G
• MyVariant Identifiers: chr1:g.67724741C>G (hg19) ; chr1:g.67259058C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259058C>G , CM000663.2:g.67259058C>G	GRCh38
NC_000001.10:g.67724741C>G , CM000663.1:g.67724741C>G	GRCh37
NC_000001.9:g.67497329C>G	NCBI36
NG_011498.1:g.97573C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1659C>G	ENSP00000513138.1:n.1659C>G
ENST00000697150.1:c.1717C>G	ENSP00000513139.1:n.1717C>G
ENST00000697151.1:c.1650C>G	ENSP00000513140.1:n.1650C>G
ENST00000697164.1:c.1730C>G	ENSP00000513153.1:p.Ser577Cys
ENST00000697165.1:c.1517C>G	ENSP00000513154.1:p.Ser506Cys
ENST00000347310.10:c.1820C>G MANE Select	ENSP00000321345.5:p.Ser607Cys
ENST00000637002.1:c.1211C>G	ENSP00000490340.1:p.Ser404Cys
ENST00000347310.9:c.1820C>G	ENSP00000321345.5:p.Ser607Cys
ENST00000395227.2:c.614C>G	ENSP00000378652.2:p.Ser205Cys
ENST00000425614.3:c.1055C>G	ENSP00000387640.2:p.Ser352Cys
ENST00000473881.2:c.*646C>G	ENSP00000486667.1:n.*646C>G
NM_144701.2:c.1820C>G	NP_653302.2:p.Ser607Cys
XM_005270516.2:c.1058C>G	XP_005270573.1:p.Ser353Cys
XM_011540789.1:c.1910C>G	XP_011539091.1:p.Ser637Cys
XM_011540790.1:c.1820C>G	XP_011539092.1:p.Ser607Cys
XM_011540791.1:c.1820C>G	XP_011539093.1:p.Ser607Cys
XM_011540790.3:c.1820C>G	XP_011539092.1:p.Ser607Cys
XM_011540791.3:c.1820C>G	XP_011539093.1:p.Ser607Cys
XR_001736993.1:n.1900C>G
NM_144701.3:c.1820C>G MANE Select	NP_653302.2:p.Ser607Cys