Canonical Allele Identifier: CA340728699

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724472C>G (hg19) ; chr1:g.67258789C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258789C>G , CM000663.2:g.67258789C>G	GRCh38
NC_000001.10:g.67724472C>G , CM000663.1:g.67724472C>G	GRCh37
NC_000001.9:g.67497060C>G	NCBI36
NG_011498.1:g.97304C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1390C>G	ENSP00000513138.1:n.1390C>G
ENST00000697150.1:c.1448C>G	ENSP00000513139.1:n.1448C>G
ENST00000697151.1:c.1381C>G	ENSP00000513140.1:n.1381C>G
ENST00000697164.1:c.1461C>G	ENSP00000513153.1:p.Asp487Glu
ENST00000697165.1:c.1248C>G	ENSP00000513154.1:p.Asp416Glu
ENST00000347310.10:c.1551C>G MANE Select	ENSP00000321345.5:p.Asp517Glu
ENST00000637002.1:c.942C>G	ENSP00000490340.1:p.Asp314Glu
ENST00000347310.9:c.1551C>G	ENSP00000321345.5:p.Asp517Glu
ENST00000395227.2:c.345C>G	ENSP00000378652.2:p.Asp115Glu
ENST00000425614.3:c.786C>G	ENSP00000387640.2:p.Asp262Glu
ENST00000473881.2:c.*377C>G	ENSP00000486667.1:n.*377C>G
NM_144701.2:c.1551C>G	NP_653302.2:p.Asp517Glu
XM_005270516.2:c.789C>G	XP_005270573.1:p.Asp263Glu
XM_011540789.1:c.1641C>G	XP_011539091.1:p.Asp547Glu
XM_011540790.1:c.1551C>G	XP_011539092.1:p.Asp517Glu
XM_011540791.1:c.1551C>G	XP_011539093.1:p.Asp517Glu
XM_011540790.3:c.1551C>G	XP_011539092.1:p.Asp517Glu
XM_011540791.3:c.1551C>G	XP_011539093.1:p.Asp517Glu
XR_001736993.1:n.1631C>G
NM_144701.3:c.1551C>G MANE Select	NP_653302.2:p.Asp517Glu