Canonical Allele Identifier: CA340729859

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724758C>G (hg19) ; chr1:g.67259075C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259075C>G , CM000663.2:g.67259075C>G	GRCh38
NC_000001.10:g.67724758C>G , CM000663.1:g.67724758C>G	GRCh37
NC_000001.9:g.67497346C>G	NCBI36
NG_011498.1:g.97590C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1676C>G	ENSP00000513138.1:n.1676C>G
ENST00000697150.1:c.1734C>G	ENSP00000513139.1:n.1734C>G
ENST00000697151.1:c.1667C>G	ENSP00000513140.1:n.1667C>G
ENST00000697164.1:c.1747C>G	ENSP00000513153.1:p.Pro583Ala
ENST00000697165.1:c.1534C>G	ENSP00000513154.1:p.Pro512Ala
ENST00000347310.10:c.1837C>G MANE Select	ENSP00000321345.5:p.Pro613Ala
ENST00000637002.1:c.1228C>G	ENSP00000490340.1:p.Pro410Ala
ENST00000347310.9:c.1837C>G	ENSP00000321345.5:p.Pro613Ala
ENST00000395227.2:c.631C>G	ENSP00000378652.2:p.Pro211Ala
ENST00000425614.3:c.1072C>G	ENSP00000387640.2:p.Pro358Ala
ENST00000473881.2:c.*663C>G	ENSP00000486667.1:n.*663C>G
NM_144701.2:c.1837C>G	NP_653302.2:p.Pro613Ala
XM_005270516.2:c.1075C>G	XP_005270573.1:p.Pro359Ala
XM_011540789.1:c.1927C>G	XP_011539091.1:p.Pro643Ala
XM_011540790.1:c.1837C>G	XP_011539092.1:p.Pro613Ala
XM_011540791.1:c.1837C>G	XP_011539093.1:p.Pro613Ala
XM_011540790.3:c.1837C>G	XP_011539092.1:p.Pro613Ala
XM_011540791.3:c.1837C>G	XP_011539093.1:p.Pro613Ala
XR_001736993.1:n.1917C>G
NM_144701.3:c.1837C>G MANE Select	NP_653302.2:p.Pro613Ala