Canonical Allele Identifier: CA340728628

Gene: IL23R

Linked Data

• dbSNP Id: rs1283551780
• MyVariant Identifiers: chr1:g.67724438C>T (hg19) ; chr1:g.67258755C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258755C>T , CM000663.2:g.67258755C>T	GRCh38
NC_000001.10:g.67724438C>T , CM000663.1:g.67724438C>T	GRCh37
NC_000001.9:g.67497026C>T	NCBI36
NG_011498.1:g.97270C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1356C>T	ENSP00000513138.1:n.1356C>T
ENST00000697150.1:c.1414C>T	ENSP00000513139.1:n.1414C>T
ENST00000697151.1:c.1347C>T	ENSP00000513140.1:n.1347C>T
ENST00000697164.1:c.1427C>T	ENSP00000513153.1:p.Ser476Phe
ENST00000697165.1:c.1214C>T	ENSP00000513154.1:p.Ser405Phe
ENST00000347310.10:c.1517C>T MANE Select	ENSP00000321345.5:p.Ser506Phe
ENST00000637002.1:c.908C>T	ENSP00000490340.1:p.Ser303Phe
ENST00000347310.9:c.1517C>T	ENSP00000321345.5:p.Ser506Phe
ENST00000395227.2:c.311C>T	ENSP00000378652.2:p.Ser104Phe
ENST00000425614.3:c.752C>T	ENSP00000387640.2:p.Ser251Phe
ENST00000473881.2:c.*343C>T	ENSP00000486667.1:n.*343C>T
NM_144701.2:c.1517C>T	NP_653302.2:p.Ser506Phe
XM_005270516.2:c.755C>T	XP_005270573.1:p.Ser252Phe
XM_011540789.1:c.1607C>T	XP_011539091.1:p.Ser536Phe
XM_011540790.1:c.1517C>T	XP_011539092.1:p.Ser506Phe
XM_011540791.1:c.1517C>T	XP_011539093.1:p.Ser506Phe
XM_011540790.3:c.1517C>T	XP_011539092.1:p.Ser506Phe
XM_011540791.3:c.1517C>T	XP_011539093.1:p.Ser506Phe
XR_001736993.1:n.1597C>T
NM_144701.3:c.1517C>T MANE Select	NP_653302.2:p.Ser506Phe