Canonical Allele Identifier: CA340728733

Gene: IL23R

Linked Data

• COSMIC: COSM6127167
• MyVariant Identifiers: chr1:g.67724488A>T (hg19) ; chr1:g.67258805A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258805A>T , CM000663.2:g.67258805A>T	GRCh38
NC_000001.10:g.67724488A>T , CM000663.1:g.67724488A>T	GRCh37
NC_000001.9:g.67497076A>T	NCBI36
NG_011498.1:g.97320A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1406A>T	ENSP00000513138.1:n.1406A>T
ENST00000697150.1:c.1464A>T	ENSP00000513139.1:n.1464A>T
ENST00000697151.1:c.1397A>T	ENSP00000513140.1:n.1397A>T
ENST00000697164.1:c.1477A>T	ENSP00000513153.1:p.Arg493Trp
ENST00000697165.1:c.1264A>T	ENSP00000513154.1:p.Arg422Trp
ENST00000347310.10:c.1567A>T MANE Select	ENSP00000321345.5:p.Arg523Trp
ENST00000637002.1:c.958A>T	ENSP00000490340.1:p.Arg320Trp
ENST00000347310.9:c.1567A>T	ENSP00000321345.5:p.Arg523Trp
ENST00000395227.2:c.361A>T	ENSP00000378652.2:p.Arg121Trp
ENST00000425614.3:c.802A>T	ENSP00000387640.2:p.Arg268Trp
ENST00000473881.2:c.*393A>T	ENSP00000486667.1:n.*393A>T
NM_144701.2:c.1567A>T	NP_653302.2:p.Arg523Trp
XM_005270516.2:c.805A>T	XP_005270573.1:p.Arg269Trp
XM_011540789.1:c.1657A>T	XP_011539091.1:p.Arg553Trp
XM_011540790.1:c.1567A>T	XP_011539092.1:p.Arg523Trp
XM_011540791.1:c.1567A>T	XP_011539093.1:p.Arg523Trp
XM_011540790.3:c.1567A>T	XP_011539092.1:p.Arg523Trp
XM_011540791.3:c.1567A>T	XP_011539093.1:p.Arg523Trp
XR_001736993.1:n.1647A>T
NM_144701.3:c.1567A>T MANE Select	NP_653302.2:p.Arg523Trp