Canonical Allele Identifier: CA340729551

Gene: IL23R

Linked Data

• dbSNP Id: rs1436667845
• gnomAD v3: 1-67259004-T-G
• gnomAD v4: 1-67259004-T-G
• MyVariant Identifiers: chr1:g.67724687T>G (hg19) ; chr1:g.67259004T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259004T>G , CM000663.2:g.67259004T>G	GRCh38
NC_000001.10:g.67724687T>G , CM000663.1:g.67724687T>G	GRCh37
NC_000001.9:g.67497275T>G	NCBI36
NG_011498.1:g.97519T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1605T>G	ENSP00000513138.1:n.1605T>G
ENST00000697150.1:c.1663T>G	ENSP00000513139.1:n.1663T>G
ENST00000697151.1:c.1596T>G	ENSP00000513140.1:n.1596T>G
ENST00000697164.1:c.1676T>G	ENSP00000513153.1:p.Leu559Arg
ENST00000697165.1:c.1463T>G	ENSP00000513154.1:p.Leu488Arg
ENST00000347310.10:c.1766T>G MANE Select	ENSP00000321345.5:p.Leu589Arg
ENST00000637002.1:c.1157T>G	ENSP00000490340.1:p.Leu386Arg
ENST00000347310.9:c.1766T>G	ENSP00000321345.5:p.Leu589Arg
ENST00000395227.2:c.560T>G	ENSP00000378652.2:p.Leu187Arg
ENST00000425614.3:c.1001T>G	ENSP00000387640.2:p.Leu334Arg
ENST00000473881.2:c.*592T>G	ENSP00000486667.1:n.*592T>G
NM_144701.2:c.1766T>G	NP_653302.2:p.Leu589Arg
XM_005270516.2:c.1004T>G	XP_005270573.1:p.Leu335Arg
XM_011540789.1:c.1856T>G	XP_011539091.1:p.Leu619Arg
XM_011540790.1:c.1766T>G	XP_011539092.1:p.Leu589Arg
XM_011540791.1:c.1766T>G	XP_011539093.1:p.Leu589Arg
XM_011540790.3:c.1766T>G	XP_011539092.1:p.Leu589Arg
XM_011540791.3:c.1766T>G	XP_011539093.1:p.Leu589Arg
XR_001736993.1:n.1846T>G
NM_144701.3:c.1766T>G MANE Select	NP_653302.2:p.Leu589Arg