Canonical Allele Identifier: CA340728795

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724515T>G (hg19) ; chr1:g.67258832T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258832T>G , CM000663.2:g.67258832T>G	GRCh38
NC_000001.10:g.67724515T>G , CM000663.1:g.67724515T>G	GRCh37
NC_000001.9:g.67497103T>G	NCBI36
NG_011498.1:g.97347T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1433T>G	ENSP00000513138.1:n.1433T>G
ENST00000697150.1:c.1491T>G	ENSP00000513139.1:n.1491T>G
ENST00000697151.1:c.1424T>G	ENSP00000513140.1:n.1424T>G
ENST00000697164.1:c.1504T>G	ENSP00000513153.1:p.Phe502Val
ENST00000697165.1:c.1291T>G	ENSP00000513154.1:p.Phe431Val
ENST00000347310.10:c.1594T>G MANE Select	ENSP00000321345.5:p.Phe532Val
ENST00000637002.1:c.985T>G	ENSP00000490340.1:p.Phe329Val
ENST00000347310.9:c.1594T>G	ENSP00000321345.5:p.Phe532Val
ENST00000395227.2:c.388T>G	ENSP00000378652.2:p.Phe130Val
ENST00000425614.3:c.829T>G	ENSP00000387640.2:p.Phe277Val
ENST00000473881.2:c.*420T>G	ENSP00000486667.1:n.*420T>G
NM_144701.2:c.1594T>G	NP_653302.2:p.Phe532Val
XM_005270516.2:c.832T>G	XP_005270573.1:p.Phe278Val
XM_011540789.1:c.1684T>G	XP_011539091.1:p.Phe562Val
XM_011540790.1:c.1594T>G	XP_011539092.1:p.Phe532Val
XM_011540791.1:c.1594T>G	XP_011539093.1:p.Phe532Val
XM_011540790.3:c.1594T>G	XP_011539092.1:p.Phe532Val
XM_011540791.3:c.1594T>G	XP_011539093.1:p.Phe532Val
XR_001736993.1:n.1674T>G
NM_144701.3:c.1594T>G MANE Select	NP_653302.2:p.Phe532Val