Canonical Allele Identifier: CA340729638

Gene: IL23R

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1629G>T	ENSP00000513138.1:n.1629G>T
ENST00000697150.1:c.1687G>T	ENSP00000513139.1:n.1687G>T
ENST00000697151.1:c.1620G>T	ENSP00000513140.1:n.1620G>T
ENST00000697164.1:c.1700G>T	ENSP00000513153.1:p.Cys567Phe
ENST00000697165.1:c.1487G>T	ENSP00000513154.1:p.Cys496Phe
ENST00000347310.10:c.1790G>T MANE Select	ENSP00000321345.5:p.Cys597Phe
ENST00000637002.1:c.1181G>T	ENSP00000490340.1:p.Cys394Phe
ENST00000347310.9:c.1790G>T	ENSP00000321345.5:p.Cys597Phe
ENST00000395227.2:c.584G>T	ENSP00000378652.2:p.Cys195Phe
ENST00000425614.3:c.1025G>T	ENSP00000387640.2:p.Cys342Phe
ENST00000473881.2:c.*616G>T	ENSP00000486667.1:n.*616G>T
NM_144701.2:c.1790G>T	NP_653302.2:p.Cys597Phe
XM_005270516.2:c.1028G>T	XP_005270573.1:p.Cys343Phe
XM_011540789.1:c.1880G>T	XP_011539091.1:p.Cys627Phe
XM_011540790.1:c.1790G>T	XP_011539092.1:p.Cys597Phe
XM_011540791.1:c.1790G>T	XP_011539093.1:p.Cys597Phe
XM_011540790.3:c.1790G>T	XP_011539092.1:p.Cys597Phe
XM_011540791.3:c.1790G>T	XP_011539093.1:p.Cys597Phe
XR_001736993.1:n.1870G>T
NM_144701.3:c.1790G>T MANE Select	NP_653302.2:p.Cys597Phe