Canonical Allele Identifier: CA340728745

Gene: IL23R

Linked Data

• gnomAD v4: 1-67258810-A-T
• MyVariant Identifiers: chr1:g.67724493A>T (hg19) ; chr1:g.67258810A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258810A>T , CM000663.2:g.67258810A>T	GRCh38
NC_000001.10:g.67724493A>T , CM000663.1:g.67724493A>T	GRCh37
NC_000001.9:g.67497081A>T	NCBI36
NG_011498.1:g.97325A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1411A>T	ENSP00000513138.1:n.1411A>T
ENST00000697150.1:c.1469A>T	ENSP00000513139.1:n.1469A>T
ENST00000697151.1:c.1402A>T	ENSP00000513140.1:n.1402A>T
ENST00000697164.1:c.1482A>T	ENSP00000513153.1:p.Leu494Phe
ENST00000697165.1:c.1269A>T	ENSP00000513154.1:p.Leu423Phe
ENST00000347310.10:c.1572A>T MANE Select	ENSP00000321345.5:p.Leu524Phe
ENST00000637002.1:c.963A>T	ENSP00000490340.1:p.Leu321Phe
ENST00000347310.9:c.1572A>T	ENSP00000321345.5:p.Leu524Phe
ENST00000395227.2:c.366A>T	ENSP00000378652.2:p.Leu122Phe
ENST00000425614.3:c.807A>T	ENSP00000387640.2:p.Leu269Phe
ENST00000473881.2:c.*398A>T	ENSP00000486667.1:n.*398A>T
NM_144701.2:c.1572A>T	NP_653302.2:p.Leu524Phe
XM_005270516.2:c.810A>T	XP_005270573.1:p.Leu270Phe
XM_011540789.1:c.1662A>T	XP_011539091.1:p.Leu554Phe
XM_011540790.1:c.1572A>T	XP_011539092.1:p.Leu524Phe
XM_011540791.1:c.1572A>T	XP_011539093.1:p.Leu524Phe
XM_011540790.3:c.1572A>T	XP_011539092.1:p.Leu524Phe
XM_011540791.3:c.1572A>T	XP_011539093.1:p.Leu524Phe
XR_001736993.1:n.1652A>T
NM_144701.3:c.1572A>T MANE Select	NP_653302.2:p.Leu524Phe