Canonical Allele Identifier: CA340728614

Gene: IL23R

Linked Data

• dbSNP Id: rs1653088350
• MyVariant Identifiers: chr1:g.67724431A>G (hg19) ; chr1:g.67258748A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258748A>G , CM000663.2:g.67258748A>G	GRCh38
NC_000001.10:g.67724431A>G , CM000663.1:g.67724431A>G	GRCh37
NC_000001.9:g.67497019A>G	NCBI36
NG_011498.1:g.97263A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1349A>G	ENSP00000513138.1:n.1349A>G
ENST00000697150.1:c.1407A>G	ENSP00000513139.1:n.1407A>G
ENST00000697151.1:c.1340A>G	ENSP00000513140.1:n.1340A>G
ENST00000697164.1:c.1420A>G	ENSP00000513153.1:p.Ile474Val
ENST00000697165.1:c.1207A>G	ENSP00000513154.1:p.Ile403Val
ENST00000347310.10:c.1510A>G MANE Select	ENSP00000321345.5:p.Ile504Val
ENST00000637002.1:c.901A>G	ENSP00000490340.1:p.Ile301Val
ENST00000347310.9:c.1510A>G	ENSP00000321345.5:p.Ile504Val
ENST00000395227.2:c.304A>G	ENSP00000378652.2:p.Ile102Val
ENST00000425614.3:c.745A>G	ENSP00000387640.2:p.Ile249Val
ENST00000473881.2:c.*336A>G	ENSP00000486667.1:n.*336A>G
NM_144701.2:c.1510A>G	NP_653302.2:p.Ile504Val
XM_005270516.2:c.748A>G	XP_005270573.1:p.Ile250Val
XM_011540789.1:c.1600A>G	XP_011539091.1:p.Ile534Val
XM_011540790.1:c.1510A>G	XP_011539092.1:p.Ile504Val
XM_011540791.1:c.1510A>G	XP_011539093.1:p.Ile504Val
XM_011540790.3:c.1510A>G	XP_011539092.1:p.Ile504Val
XM_011540791.3:c.1510A>G	XP_011539093.1:p.Ile504Val
XR_001736993.1:n.1590A>G
NM_144701.3:c.1510A>G MANE Select	NP_653302.2:p.Ile504Val