Canonical Allele Identifier: CA340729175

Gene: IL23R

Linked Data

• gnomAD v4: 1-67258910-T-G
• MyVariant Identifiers: chr1:g.67724593T>G (hg19) ; chr1:g.67258910T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258910T>G , CM000663.2:g.67258910T>G	GRCh38
NC_000001.10:g.67724593T>G , CM000663.1:g.67724593T>G	GRCh37
NC_000001.9:g.67497181T>G	NCBI36
NG_011498.1:g.97425T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1511T>G	ENSP00000513138.1:n.1511T>G
ENST00000697150.1:c.1569T>G	ENSP00000513139.1:n.1569T>G
ENST00000697151.1:c.1502T>G	ENSP00000513140.1:n.1502T>G
ENST00000697164.1:c.1582T>G	ENSP00000513153.1:p.Cys528Gly
ENST00000697165.1:c.1369T>G	ENSP00000513154.1:p.Cys457Gly
ENST00000347310.10:c.1672T>G MANE Select	ENSP00000321345.5:p.Cys558Gly
ENST00000637002.1:c.1063T>G	ENSP00000490340.1:p.Cys355Gly
ENST00000347310.9:c.1672T>G	ENSP00000321345.5:p.Cys558Gly
ENST00000395227.2:c.466T>G	ENSP00000378652.2:p.Cys156Gly
ENST00000425614.3:c.907T>G	ENSP00000387640.2:p.Cys303Gly
ENST00000473881.2:c.*498T>G	ENSP00000486667.1:n.*498T>G
NM_144701.2:c.1672T>G	NP_653302.2:p.Cys558Gly
XM_005270516.2:c.910T>G	XP_005270573.1:p.Cys304Gly
XM_011540789.1:c.1762T>G	XP_011539091.1:p.Cys588Gly
XM_011540790.1:c.1672T>G	XP_011539092.1:p.Cys558Gly
XM_011540791.1:c.1672T>G	XP_011539093.1:p.Cys558Gly
XM_011540790.3:c.1672T>G	XP_011539092.1:p.Cys558Gly
XM_011540791.3:c.1672T>G	XP_011539093.1:p.Cys558Gly
XR_001736993.1:n.1752T>G
NM_144701.3:c.1672T>G MANE Select	NP_653302.2:p.Cys558Gly