Canonical Allele Identifier: CA340728801

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724517T>G (hg19) ; chr1:g.67258834T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258834T>G , CM000663.2:g.67258834T>G	GRCh38
NC_000001.10:g.67724517T>G , CM000663.1:g.67724517T>G	GRCh37
NC_000001.9:g.67497105T>G	NCBI36
NG_011498.1:g.97349T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1435T>G	ENSP00000513138.1:n.1435T>G
ENST00000697150.1:c.1493T>G	ENSP00000513139.1:n.1493T>G
ENST00000697151.1:c.1426T>G	ENSP00000513140.1:n.1426T>G
ENST00000697164.1:c.1506T>G	ENSP00000513153.1:p.Phe502Leu
ENST00000697165.1:c.1293T>G	ENSP00000513154.1:p.Phe431Leu
ENST00000347310.10:c.1596T>G MANE Select	ENSP00000321345.5:p.Phe532Leu
ENST00000637002.1:c.987T>G	ENSP00000490340.1:p.Phe329Leu
ENST00000347310.9:c.1596T>G	ENSP00000321345.5:p.Phe532Leu
ENST00000395227.2:c.390T>G	ENSP00000378652.2:p.Phe130Leu
ENST00000425614.3:c.831T>G	ENSP00000387640.2:p.Phe277Leu
ENST00000473881.2:c.*422T>G	ENSP00000486667.1:n.*422T>G
NM_144701.2:c.1596T>G	NP_653302.2:p.Phe532Leu
XM_005270516.2:c.834T>G	XP_005270573.1:p.Phe278Leu
XM_011540789.1:c.1686T>G	XP_011539091.1:p.Phe562Leu
XM_011540790.1:c.1596T>G	XP_011539092.1:p.Phe532Leu
XM_011540791.1:c.1596T>G	XP_011539093.1:p.Phe532Leu
XM_011540790.3:c.1596T>G	XP_011539092.1:p.Phe532Leu
XM_011540791.3:c.1596T>G	XP_011539093.1:p.Phe532Leu
XR_001736993.1:n.1676T>G
NM_144701.3:c.1596T>G MANE Select	NP_653302.2:p.Phe532Leu