Canonical Allele Identifier: CA340728793

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724513C>G (hg19) ; chr1:g.67258830C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258830C>G , CM000663.2:g.67258830C>G	GRCh38
NC_000001.10:g.67724513C>G , CM000663.1:g.67724513C>G	GRCh37
NC_000001.9:g.67497101C>G	NCBI36
NG_011498.1:g.97345C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1431C>G	ENSP00000513138.1:n.1431C>G
ENST00000697150.1:c.1489C>G	ENSP00000513139.1:n.1489C>G
ENST00000697151.1:c.1422C>G	ENSP00000513140.1:n.1422C>G
ENST00000697164.1:c.1502C>G	ENSP00000513153.1:p.Ala501Gly
ENST00000697165.1:c.1289C>G	ENSP00000513154.1:p.Ala430Gly
ENST00000347310.10:c.1592C>G MANE Select	ENSP00000321345.5:p.Ala531Gly
ENST00000637002.1:c.983C>G	ENSP00000490340.1:p.Ala328Gly
ENST00000347310.9:c.1592C>G	ENSP00000321345.5:p.Ala531Gly
ENST00000395227.2:c.386C>G	ENSP00000378652.2:p.Ala129Gly
ENST00000425614.3:c.827C>G	ENSP00000387640.2:p.Ala276Gly
ENST00000473881.2:c.*418C>G	ENSP00000486667.1:n.*418C>G
NM_144701.2:c.1592C>G	NP_653302.2:p.Ala531Gly
XM_005270516.2:c.830C>G	XP_005270573.1:p.Ala277Gly
XM_011540789.1:c.1682C>G	XP_011539091.1:p.Ala561Gly
XM_011540790.1:c.1592C>G	XP_011539092.1:p.Ala531Gly
XM_011540791.1:c.1592C>G	XP_011539093.1:p.Ala531Gly
XM_011540790.3:c.1592C>G	XP_011539092.1:p.Ala531Gly
XM_011540791.3:c.1592C>G	XP_011539093.1:p.Ala531Gly
XR_001736993.1:n.1672C>G
NM_144701.3:c.1592C>G MANE Select	NP_653302.2:p.Ala531Gly