Canonical Allele Identifier: CA340728840

Gene: IL23R

Linked Data

• gnomAD v4: 1-67258847-G-T
• MyVariant Identifiers: chr1:g.67724530G>T (hg19) ; chr1:g.67258847G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258847G>T , CM000663.2:g.67258847G>T	GRCh38
NC_000001.10:g.67724530G>T , CM000663.1:g.67724530G>T	GRCh37
NC_000001.9:g.67497118G>T	NCBI36
NG_011498.1:g.97362G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1448G>T	ENSP00000513138.1:n.1448G>T
ENST00000697150.1:c.1506G>T	ENSP00000513139.1:n.1506G>T
ENST00000697151.1:c.1439G>T	ENSP00000513140.1:n.1439G>T
ENST00000697164.1:c.1519G>T	ENSP00000513153.1:p.Val507Leu
ENST00000697165.1:c.1306G>T	ENSP00000513154.1:p.Val436Leu
ENST00000347310.10:c.1609G>T MANE Select	ENSP00000321345.5:p.Val537Leu
ENST00000637002.1:c.1000G>T	ENSP00000490340.1:p.Val334Leu
ENST00000347310.9:c.1609G>T	ENSP00000321345.5:p.Val537Leu
ENST00000395227.2:c.403G>T	ENSP00000378652.2:p.Val135Leu
ENST00000425614.3:c.844G>T	ENSP00000387640.2:p.Val282Leu
ENST00000473881.2:c.*435G>T	ENSP00000486667.1:n.*435G>T
NM_144701.2:c.1609G>T	NP_653302.2:p.Val537Leu
XM_005270516.2:c.847G>T	XP_005270573.1:p.Val283Leu
XM_011540789.1:c.1699G>T	XP_011539091.1:p.Val567Leu
XM_011540790.1:c.1609G>T	XP_011539092.1:p.Val537Leu
XM_011540791.1:c.1609G>T	XP_011539093.1:p.Val537Leu
XM_011540790.3:c.1609G>T	XP_011539092.1:p.Val537Leu
XM_011540791.3:c.1609G>T	XP_011539093.1:p.Val537Leu
XR_001736993.1:n.1689G>T
NM_144701.3:c.1609G>T MANE Select	NP_653302.2:p.Val537Leu