Canonical Allele Identifier: CA418438787

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724541A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258858A>G , CM000663.2:g.67258858A>G	GRCh38
NC_000001.10:g.67724541A>G , CM000663.1:g.67724541A>G	GRCh37
NC_000001.9:g.67497129A>G	NCBI36
NG_011498.1:g.97373A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1459A>G	ENSP00000513138.1:n.1459A>G
ENST00000697150.1:c.1517A>G	ENSP00000513139.1:n.1517A>G
ENST00000697151.1:c.1450A>G	ENSP00000513140.1:n.1450A>G
ENST00000697164.1:c.1530A>G	ENSP00000513153.1:p.Leu510=
ENST00000697165.1:c.1317A>G	ENSP00000513154.1:p.Leu439=
ENST00000347310.10:c.1620A>G MANE Select	ENSP00000321345.5:p.Leu540=
ENST00000637002.1:c.1011A>G	ENSP00000490340.1:p.Leu337=
ENST00000347310.9:c.1620A>G	ENSP00000321345.5:p.Leu540=
ENST00000395227.2:c.414A>G	ENSP00000378652.2:p.Leu138=
ENST00000425614.3:c.855A>G	ENSP00000387640.2:p.Leu285=
ENST00000473881.2:c.*446A>G	ENSP00000486667.1:n.*446A>G
NM_144701.2:c.1620A>G	NP_653302.2:p.Leu540=
XM_005270516.2:c.858A>G	XP_005270573.1:p.Leu286=
XM_011540789.1:c.1710A>G	XP_011539091.1:p.Leu570=
XM_011540790.1:c.1620A>G	XP_011539092.1:p.Leu540=
XM_011540791.1:c.1620A>G	XP_011539093.1:p.Leu540=
XM_011540790.3:c.1620A>G	XP_011539092.1:p.Leu540=
XM_011540791.3:c.1620A>G	XP_011539093.1:p.Leu540=
XR_001736993.1:n.1700A>G
NM_144701.3:c.1620A>G MANE Select	NP_653302.2:p.Leu540=