Canonical Allele Identifier: CA418438611

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724601T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258918T>G , CM000663.2:g.67258918T>G	GRCh38
NC_000001.10:g.67724601T>G , CM000663.1:g.67724601T>G	GRCh37
NC_000001.9:g.67497189T>G	NCBI36
NG_011498.1:g.97433T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1519T>G	ENSP00000513138.1:n.1519T>G
ENST00000697150.1:c.1577T>G	ENSP00000513139.1:n.1577T>G
ENST00000697151.1:c.1510T>G	ENSP00000513140.1:n.1510T>G
ENST00000697164.1:c.1590T>G	ENSP00000513153.1:p.Ser530=
ENST00000697165.1:c.1377T>G	ENSP00000513154.1:p.Ser459=
ENST00000347310.10:c.1680T>G MANE Select	ENSP00000321345.5:p.Ser560=
ENST00000637002.1:c.1071T>G	ENSP00000490340.1:p.Ser357=
ENST00000347310.9:c.1680T>G	ENSP00000321345.5:p.Ser560=
ENST00000395227.2:c.474T>G	ENSP00000378652.2:p.Ser158=
ENST00000425614.3:c.915T>G	ENSP00000387640.2:p.Ser305=
ENST00000473881.2:c.*506T>G	ENSP00000486667.1:n.*506T>G
NM_144701.2:c.1680T>G	NP_653302.2:p.Ser560=
XM_005270516.2:c.918T>G	XP_005270573.1:p.Ser306=
XM_011540789.1:c.1770T>G	XP_011539091.1:p.Ser590=
XM_011540790.1:c.1680T>G	XP_011539092.1:p.Ser560=
XM_011540791.1:c.1680T>G	XP_011539093.1:p.Ser560=
XM_011540790.3:c.1680T>G	XP_011539092.1:p.Ser560=
XM_011540791.3:c.1680T>G	XP_011539093.1:p.Ser560=
XR_001736993.1:n.1760T>G
NM_144701.3:c.1680T>G MANE Select	NP_653302.2:p.Ser560=