Canonical Allele Identifier: CA418438842

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724811G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259128G>A , CM000663.2:g.67259128G>A	GRCh38
NC_000001.10:g.67724811G>A , CM000663.1:g.67724811G>A	GRCh37
NC_000001.9:g.67497399G>A	NCBI36
NG_011498.1:g.97643G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697164.1:c.1800G>A	ENSP00000513153.1:p.Ter600=
ENST00000697165.1:c.1587G>A	ENSP00000513154.1:p.Ter529=
ENST00000347310.10:c.1890G>A MANE Select	ENSP00000321345.5:p.Ter630=
ENST00000637002.1:c.1281G>A	ENSP00000490340.1:p.Ter427=
ENST00000347310.9:c.1890G>A	ENSP00000321345.5:p.Ter630=
ENST00000395227.2:c.684G>A	ENSP00000378652.2:p.Ter228=
ENST00000425614.3:c.1125G>A	ENSP00000387640.2:p.Ter375=
ENST00000473881.2:c.*716G>A	ENSP00000486667.1:n.*716G>A
NM_144701.2:c.1890G>A	NP_653302.2:p.Ter630=
XM_005270516.2:c.1128G>A	XP_005270573.1:p.Ter376=
XM_011540789.1:c.1980G>A	XP_011539091.1:p.Ter660=
XM_011540790.1:c.1890G>A	XP_011539092.1:p.Ter630=
XM_011540791.1:c.1890G>A	XP_011539093.1:p.Ter630=
XM_011540790.3:c.1890G>A	XP_011539092.1:p.Ter630=
XM_011540791.3:c.1890G>A	XP_011539093.1:p.Ter630=
NM_144701.3:c.1890G>A MANE Select	NP_653302.2:p.Ter630=