Canonical Allele Identifier: CA418438722

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724487C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258804C>G , CM000663.2:g.67258804C>G	GRCh38
NC_000001.10:g.67724487C>G , CM000663.1:g.67724487C>G	GRCh37
NC_000001.9:g.67497075C>G	NCBI36
NG_011498.1:g.97319C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1405C>G	ENSP00000513138.1:n.1405C>G
ENST00000697150.1:c.1463C>G	ENSP00000513139.1:n.1463C>G
ENST00000697151.1:c.1396C>G	ENSP00000513140.1:n.1396C>G
ENST00000697164.1:c.1476C>G	ENSP00000513153.1:p.Pro492=
ENST00000697165.1:c.1263C>G	ENSP00000513154.1:p.Pro421=
ENST00000347310.10:c.1566C>G MANE Select	ENSP00000321345.5:p.Pro522=
ENST00000637002.1:c.957C>G	ENSP00000490340.1:p.Pro319=
ENST00000347310.9:c.1566C>G	ENSP00000321345.5:p.Pro522=
ENST00000395227.2:c.360C>G	ENSP00000378652.2:p.Pro120=
ENST00000425614.3:c.801C>G	ENSP00000387640.2:p.Pro267=
ENST00000473881.2:c.*392C>G	ENSP00000486667.1:n.*392C>G
NM_144701.2:c.1566C>G	NP_653302.2:p.Pro522=
XM_005270516.2:c.804C>G	XP_005270573.1:p.Pro268=
XM_011540789.1:c.1656C>G	XP_011539091.1:p.Pro552=
XM_011540790.1:c.1566C>G	XP_011539092.1:p.Pro522=
XM_011540791.1:c.1566C>G	XP_011539093.1:p.Pro522=
XM_011540790.3:c.1566C>G	XP_011539092.1:p.Pro522=
XM_011540791.3:c.1566C>G	XP_011539093.1:p.Pro522=
XR_001736993.1:n.1646C>G
NM_144701.3:c.1566C>G MANE Select	NP_653302.2:p.Pro522=