Canonical Allele Identifier: CA340728800

Gene: IL23R

Linked Data

• dbSNP Id: rs1400483678
• gnomAD v2: 1-67724517-T-A
• gnomAD v4: 1-67258834-T-A
• MyVariant Identifiers: chr1:g.67724517T>A (hg19) ; chr1:g.67258834T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258834T>A , CM000663.2:g.67258834T>A	GRCh38
NC_000001.10:g.67724517T>A , CM000663.1:g.67724517T>A	GRCh37
NC_000001.9:g.67497105T>A	NCBI36
NG_011498.1:g.97349T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1435T>A	ENSP00000513138.1:n.1435T>A
ENST00000697150.1:c.1493T>A	ENSP00000513139.1:n.1493T>A
ENST00000697151.1:c.1426T>A	ENSP00000513140.1:n.1426T>A
ENST00000697164.1:c.1506T>A	ENSP00000513153.1:p.Phe502Leu
ENST00000697165.1:c.1293T>A	ENSP00000513154.1:p.Phe431Leu
ENST00000347310.10:c.1596T>A MANE Select	ENSP00000321345.5:p.Phe532Leu
ENST00000637002.1:c.987T>A	ENSP00000490340.1:p.Phe329Leu
ENST00000347310.9:c.1596T>A	ENSP00000321345.5:p.Phe532Leu
ENST00000395227.2:c.390T>A	ENSP00000378652.2:p.Phe130Leu
ENST00000425614.3:c.831T>A	ENSP00000387640.2:p.Phe277Leu
ENST00000473881.2:c.*422T>A	ENSP00000486667.1:n.*422T>A
NM_144701.2:c.1596T>A	NP_653302.2:p.Phe532Leu
XM_005270516.2:c.834T>A	XP_005270573.1:p.Phe278Leu
XM_011540789.1:c.1686T>A	XP_011539091.1:p.Phe562Leu
XM_011540790.1:c.1596T>A	XP_011539092.1:p.Phe532Leu
XM_011540791.1:c.1596T>A	XP_011539093.1:p.Phe532Leu
XM_011540790.3:c.1596T>A	XP_011539092.1:p.Phe532Leu
XM_011540791.3:c.1596T>A	XP_011539093.1:p.Phe532Leu
XR_001736993.1:n.1676T>A
NM_144701.3:c.1596T>A MANE Select	NP_653302.2:p.Phe532Leu