Canonical Allele Identifier: CA340728631

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724440T>G (hg19) ; chr1:g.67258757T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258757T>G , CM000663.2:g.67258757T>G	GRCh38
NC_000001.10:g.67724440T>G , CM000663.1:g.67724440T>G	GRCh37
NC_000001.9:g.67497028T>G	NCBI36
NG_011498.1:g.97272T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1358T>G	ENSP00000513138.1:n.1358T>G
ENST00000697150.1:c.1416T>G	ENSP00000513139.1:n.1416T>G
ENST00000697151.1:c.1349T>G	ENSP00000513140.1:n.1349T>G
ENST00000697164.1:c.1429T>G	ENSP00000513153.1:p.Leu477Val
ENST00000697165.1:c.1216T>G	ENSP00000513154.1:p.Leu406Val
ENST00000347310.10:c.1519T>G MANE Select	ENSP00000321345.5:p.Leu507Val
ENST00000637002.1:c.910T>G	ENSP00000490340.1:p.Leu304Val
ENST00000347310.9:c.1519T>G	ENSP00000321345.5:p.Leu507Val
ENST00000395227.2:c.313T>G	ENSP00000378652.2:p.Leu105Val
ENST00000425614.3:c.754T>G	ENSP00000387640.2:p.Leu252Val
ENST00000473881.2:c.*345T>G	ENSP00000486667.1:n.*345T>G
NM_144701.2:c.1519T>G	NP_653302.2:p.Leu507Val
XM_005270516.2:c.757T>G	XP_005270573.1:p.Leu253Val
XM_011540789.1:c.1609T>G	XP_011539091.1:p.Leu537Val
XM_011540790.1:c.1519T>G	XP_011539092.1:p.Leu507Val
XM_011540791.1:c.1519T>G	XP_011539093.1:p.Leu507Val
XM_011540790.3:c.1519T>G	XP_011539092.1:p.Leu507Val
XM_011540791.3:c.1519T>G	XP_011539093.1:p.Leu507Val
XR_001736993.1:n.1599T>G
NM_144701.3:c.1519T>G MANE Select	NP_653302.2:p.Leu507Val