Canonical Allele Identifier: CA340729861

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724759C>G (hg19) ; chr1:g.67259076C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259076C>G , CM000663.2:g.67259076C>G	GRCh38
NC_000001.10:g.67724759C>G , CM000663.1:g.67724759C>G	GRCh37
NC_000001.9:g.67497347C>G	NCBI36
NG_011498.1:g.97591C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1677C>G	ENSP00000513138.1:n.1677C>G
ENST00000697150.1:c.1735C>G	ENSP00000513139.1:n.1735C>G
ENST00000697151.1:c.1668C>G	ENSP00000513140.1:n.1668C>G
ENST00000697164.1:c.1748C>G	ENSP00000513153.1:p.Pro583Arg
ENST00000697165.1:c.1535C>G	ENSP00000513154.1:p.Pro512Arg
ENST00000347310.10:c.1838C>G MANE Select	ENSP00000321345.5:p.Pro613Arg
ENST00000637002.1:c.1229C>G	ENSP00000490340.1:p.Pro410Arg
ENST00000347310.9:c.1838C>G	ENSP00000321345.5:p.Pro613Arg
ENST00000395227.2:c.632C>G	ENSP00000378652.2:p.Pro211Arg
ENST00000425614.3:c.1073C>G	ENSP00000387640.2:p.Pro358Arg
ENST00000473881.2:c.*664C>G	ENSP00000486667.1:n.*664C>G
NM_144701.2:c.1838C>G	NP_653302.2:p.Pro613Arg
XM_005270516.2:c.1076C>G	XP_005270573.1:p.Pro359Arg
XM_011540789.1:c.1928C>G	XP_011539091.1:p.Pro643Arg
XM_011540790.1:c.1838C>G	XP_011539092.1:p.Pro613Arg
XM_011540791.1:c.1838C>G	XP_011539093.1:p.Pro613Arg
XM_011540790.3:c.1838C>G	XP_011539092.1:p.Pro613Arg
XM_011540791.3:c.1838C>G	XP_011539093.1:p.Pro613Arg
XR_001736993.1:n.1918C>G
NM_144701.3:c.1838C>G MANE Select	NP_653302.2:p.Pro613Arg