Canonical Allele Identifier: CA340730055

Gene: IL23R

Linked Data

• COSMIC: COSM5928094
• MyVariant Identifiers: chr1:g.67724789G>A (hg19) ; chr1:g.67259106G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259106G>A , CM000663.2:g.67259106G>A	GRCh38
NC_000001.10:g.67724789G>A , CM000663.1:g.67724789G>A	GRCh37
NC_000001.9:g.67497377G>A	NCBI36
NG_011498.1:g.97621G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1707G>A	ENSP00000513138.1:n.1707G>A
ENST00000697150.1:c.1765G>A	ENSP00000513139.1:n.1765G>A
ENST00000697151.1:c.1698G>A	ENSP00000513140.1:n.1698G>A
ENST00000697164.1:c.1778G>A	ENSP00000513153.1:p.Arg593Lys
ENST00000697165.1:c.1565G>A	ENSP00000513154.1:p.Arg522Lys
ENST00000347310.10:c.1868G>A MANE Select	ENSP00000321345.5:p.Arg623Lys
ENST00000637002.1:c.1259G>A	ENSP00000490340.1:p.Arg420Lys
ENST00000347310.9:c.1868G>A	ENSP00000321345.5:p.Arg623Lys
ENST00000395227.2:c.662G>A	ENSP00000378652.2:p.Arg221Lys
ENST00000425614.3:c.1103G>A	ENSP00000387640.2:p.Arg368Lys
ENST00000473881.2:c.*694G>A	ENSP00000486667.1:n.*694G>A
NM_144701.2:c.1868G>A	NP_653302.2:p.Arg623Lys
XM_005270516.2:c.1106G>A	XP_005270573.1:p.Arg369Lys
XM_011540789.1:c.1958G>A	XP_011539091.1:p.Arg653Lys
XM_011540790.1:c.1868G>A	XP_011539092.1:p.Arg623Lys
XM_011540791.1:c.1868G>A	XP_011539093.1:p.Arg623Lys
XM_011540790.3:c.1868G>A	XP_011539092.1:p.Arg623Lys
XM_011540791.3:c.1868G>A	XP_011539093.1:p.Arg623Lys
XR_001736993.1:n.1948G>A
NM_144701.3:c.1868G>A MANE Select	NP_653302.2:p.Arg623Lys