Canonical Allele Identifier: CA418438700

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724472C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258789C>T , CM000663.2:g.67258789C>T	GRCh38
NC_000001.10:g.67724472C>T , CM000663.1:g.67724472C>T	GRCh37
NC_000001.9:g.67497060C>T	NCBI36
NG_011498.1:g.97304C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1390C>T	ENSP00000513138.1:n.1390C>T
ENST00000697150.1:c.1448C>T	ENSP00000513139.1:n.1448C>T
ENST00000697151.1:c.1381C>T	ENSP00000513140.1:n.1381C>T
ENST00000697164.1:c.1461C>T	ENSP00000513153.1:p.Asp487=
ENST00000697165.1:c.1248C>T	ENSP00000513154.1:p.Asp416=
ENST00000347310.10:c.1551C>T MANE Select	ENSP00000321345.5:p.Asp517=
ENST00000637002.1:c.942C>T	ENSP00000490340.1:p.Asp314=
ENST00000347310.9:c.1551C>T	ENSP00000321345.5:p.Asp517=
ENST00000395227.2:c.345C>T	ENSP00000378652.2:p.Asp115=
ENST00000425614.3:c.786C>T	ENSP00000387640.2:p.Asp262=
ENST00000473881.2:c.*377C>T	ENSP00000486667.1:n.*377C>T
NM_144701.2:c.1551C>T	NP_653302.2:p.Asp517=
XM_005270516.2:c.789C>T	XP_005270573.1:p.Asp263=
XM_011540789.1:c.1641C>T	XP_011539091.1:p.Asp547=
XM_011540790.1:c.1551C>T	XP_011539092.1:p.Asp517=
XM_011540791.1:c.1551C>T	XP_011539093.1:p.Asp517=
XM_011540790.3:c.1551C>T	XP_011539092.1:p.Asp517=
XM_011540791.3:c.1551C>T	XP_011539093.1:p.Asp517=
XR_001736993.1:n.1631C>T
NM_144701.3:c.1551C>T MANE Select	NP_653302.2:p.Asp517=