Canonical Allele Identifier: CA340729485

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724668A>G (hg19) ; chr1:g.67258985A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258985A>G , CM000663.2:g.67258985A>G	GRCh38
NC_000001.10:g.67724668A>G , CM000663.1:g.67724668A>G	GRCh37
NC_000001.9:g.67497256A>G	NCBI36
NG_011498.1:g.97500A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1586A>G	ENSP00000513138.1:n.1586A>G
ENST00000697150.1:c.1644A>G	ENSP00000513139.1:n.1644A>G
ENST00000697151.1:c.1577A>G	ENSP00000513140.1:n.1577A>G
ENST00000697164.1:c.1657A>G	ENSP00000513153.1:p.Thr553Ala
ENST00000697165.1:c.1444A>G	ENSP00000513154.1:p.Thr482Ala
ENST00000347310.10:c.1747A>G MANE Select	ENSP00000321345.5:p.Thr583Ala
ENST00000637002.1:c.1138A>G	ENSP00000490340.1:p.Thr380Ala
ENST00000347310.9:c.1747A>G	ENSP00000321345.5:p.Thr583Ala
ENST00000395227.2:c.541A>G	ENSP00000378652.2:p.Thr181Ala
ENST00000425614.3:c.982A>G	ENSP00000387640.2:p.Thr328Ala
ENST00000473881.2:c.*573A>G	ENSP00000486667.1:n.*573A>G
NM_144701.2:c.1747A>G	NP_653302.2:p.Thr583Ala
XM_005270516.2:c.985A>G	XP_005270573.1:p.Thr329Ala
XM_011540789.1:c.1837A>G	XP_011539091.1:p.Thr613Ala
XM_011540790.1:c.1747A>G	XP_011539092.1:p.Thr583Ala
XM_011540791.1:c.1747A>G	XP_011539093.1:p.Thr583Ala
XM_011540790.3:c.1747A>G	XP_011539092.1:p.Thr583Ala
XM_011540791.3:c.1747A>G	XP_011539093.1:p.Thr583Ala
XR_001736993.1:n.1827A>G
NM_144701.3:c.1747A>G MANE Select	NP_653302.2:p.Thr583Ala