Canonical Allele Identifier: CA340730088

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724793T>G (hg19) ; chr1:g.67259110T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259110T>G , CM000663.2:g.67259110T>G	GRCh38
NC_000001.10:g.67724793T>G , CM000663.1:g.67724793T>G	GRCh37
NC_000001.9:g.67497381T>G	NCBI36
NG_011498.1:g.97625T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000697149.1:c.1711T>G	ENSP00000513138.1:n.1711T>G
ENST00000697150.1:c.1769T>G	ENSP00000513139.1:n.1769T>G
ENST00000697151.1:c.1702T>G	ENSP00000513140.1:n.1702T>G
ENST00000697164.1:c.1782T>G	ENSP00000513153.1:p.Ile594Met
ENST00000697165.1:c.1569T>G	ENSP00000513154.1:p.Ile523Met
ENST00000347310.10:c.1872T>G MANE Select	ENSP00000321345.5:p.Ile624Met
ENST00000637002.1:c.1263T>G	ENSP00000490340.1:p.Ile421Met
ENST00000347310.9:c.1872T>G	ENSP00000321345.5:p.Ile624Met
ENST00000395227.2:c.666T>G	ENSP00000378652.2:p.Ile222Met
ENST00000425614.3:c.1107T>G	ENSP00000387640.2:p.Ile369Met
ENST00000473881.2:c.*698T>G	ENSP00000486667.1:n.*698T>G
NM_144701.2:c.1872T>G	NP_653302.2:p.Ile624Met
XM_005270516.2:c.1110T>G	XP_005270573.1:p.Ile370Met
XM_011540789.1:c.1962T>G	XP_011539091.1:p.Ile654Met
XM_011540790.1:c.1872T>G	XP_011539092.1:p.Ile624Met
XM_011540791.1:c.1872T>G	XP_011539093.1:p.Ile624Met
XM_011540790.3:c.1872T>G	XP_011539092.1:p.Ile624Met
XM_011540791.3:c.1872T>G	XP_011539093.1:p.Ile624Met
XR_001736993.1:n.1952T>G
NM_144701.3:c.1872T>G MANE Select	NP_653302.2:p.Ile624Met