Canonical Allele Identifier: CA340729636

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724711G>A (hg19) ; chr1:g.67259028G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259028G>A , CM000663.2:g.67259028G>A	GRCh38
NC_000001.10:g.67724711G>A , CM000663.1:g.67724711G>A	GRCh37
NC_000001.9:g.67497299G>A	NCBI36
NG_011498.1:g.97543G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1629G>A	ENSP00000513138.1:n.1629G>A
ENST00000697150.1:c.1687G>A	ENSP00000513139.1:n.1687G>A
ENST00000697151.1:c.1620G>A	ENSP00000513140.1:n.1620G>A
ENST00000697164.1:c.1700G>A	ENSP00000513153.1:p.Cys567Tyr
ENST00000697165.1:c.1487G>A	ENSP00000513154.1:p.Cys496Tyr
ENST00000347310.10:c.1790G>A MANE Select	ENSP00000321345.5:p.Cys597Tyr
ENST00000637002.1:c.1181G>A	ENSP00000490340.1:p.Cys394Tyr
ENST00000347310.9:c.1790G>A	ENSP00000321345.5:p.Cys597Tyr
ENST00000395227.2:c.584G>A	ENSP00000378652.2:p.Cys195Tyr
ENST00000425614.3:c.1025G>A	ENSP00000387640.2:p.Cys342Tyr
ENST00000473881.2:c.*616G>A	ENSP00000486667.1:n.*616G>A
NM_144701.2:c.1790G>A	NP_653302.2:p.Cys597Tyr
XM_005270516.2:c.1028G>A	XP_005270573.1:p.Cys343Tyr
XM_011540789.1:c.1880G>A	XP_011539091.1:p.Cys627Tyr
XM_011540790.1:c.1790G>A	XP_011539092.1:p.Cys597Tyr
XM_011540791.1:c.1790G>A	XP_011539093.1:p.Cys597Tyr
XM_011540790.3:c.1790G>A	XP_011539092.1:p.Cys597Tyr
XM_011540791.3:c.1790G>A	XP_011539093.1:p.Cys597Tyr
XR_001736993.1:n.1870G>A
NM_144701.3:c.1790G>A MANE Select	NP_653302.2:p.Cys597Tyr