Canonical Allele Identifier: CA340729542

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724684C>G (hg19) ; chr1:g.67259001C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259001C>G , CM000663.2:g.67259001C>G	GRCh38
NC_000001.10:g.67724684C>G , CM000663.1:g.67724684C>G	GRCh37
NC_000001.9:g.67497272C>G	NCBI36
NG_011498.1:g.97516C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1602C>G	ENSP00000513138.1:n.1602C>G
ENST00000697150.1:c.1660C>G	ENSP00000513139.1:n.1660C>G
ENST00000697151.1:c.1593C>G	ENSP00000513140.1:n.1593C>G
ENST00000697164.1:c.1673C>G	ENSP00000513153.1:p.Thr558Ser
ENST00000697165.1:c.1460C>G	ENSP00000513154.1:p.Thr487Ser
ENST00000347310.10:c.1763C>G MANE Select	ENSP00000321345.5:p.Thr588Ser
ENST00000637002.1:c.1154C>G	ENSP00000490340.1:p.Thr385Ser
ENST00000347310.9:c.1763C>G	ENSP00000321345.5:p.Thr588Ser
ENST00000395227.2:c.557C>G	ENSP00000378652.2:p.Thr186Ser
ENST00000425614.3:c.998C>G	ENSP00000387640.2:p.Thr333Ser
ENST00000473881.2:c.*589C>G	ENSP00000486667.1:n.*589C>G
NM_144701.2:c.1763C>G	NP_653302.2:p.Thr588Ser
XM_005270516.2:c.1001C>G	XP_005270573.1:p.Thr334Ser
XM_011540789.1:c.1853C>G	XP_011539091.1:p.Thr618Ser
XM_011540790.1:c.1763C>G	XP_011539092.1:p.Thr588Ser
XM_011540791.1:c.1763C>G	XP_011539093.1:p.Thr588Ser
XM_011540790.3:c.1763C>G	XP_011539092.1:p.Thr588Ser
XM_011540791.3:c.1763C>G	XP_011539093.1:p.Thr588Ser
XR_001736993.1:n.1843C>G
NM_144701.3:c.1763C>G MANE Select	NP_653302.2:p.Thr588Ser