Canonical Allele Identifier: CA340728772

Gene: IL23R

Linked Data

• gnomAD v4: 1-67258821-C-A
• MyVariant Identifiers: chr1:g.67724504C>A (hg19) ; chr1:g.67258821C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258821C>A , CM000663.2:g.67258821C>A	GRCh38
NC_000001.10:g.67724504C>A , CM000663.1:g.67724504C>A	GRCh37
NC_000001.9:g.67497092C>A	NCBI36
NG_011498.1:g.97336C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1422C>A	ENSP00000513138.1:n.1422C>A
ENST00000697150.1:c.1480C>A	ENSP00000513139.1:n.1480C>A
ENST00000697151.1:c.1413C>A	ENSP00000513140.1:n.1413C>A
ENST00000697164.1:c.1493C>A	ENSP00000513153.1:p.Pro498His
ENST00000697165.1:c.1280C>A	ENSP00000513154.1:p.Pro427His
ENST00000347310.10:c.1583C>A MANE Select	ENSP00000321345.5:p.Pro528His
ENST00000637002.1:c.974C>A	ENSP00000490340.1:p.Pro325His
ENST00000347310.9:c.1583C>A	ENSP00000321345.5:p.Pro528His
ENST00000395227.2:c.377C>A	ENSP00000378652.2:p.Pro126His
ENST00000425614.3:c.818C>A	ENSP00000387640.2:p.Pro273His
ENST00000473881.2:c.*409C>A	ENSP00000486667.1:n.*409C>A
NM_144701.2:c.1583C>A	NP_653302.2:p.Pro528His
XM_005270516.2:c.821C>A	XP_005270573.1:p.Pro274His
XM_011540789.1:c.1673C>A	XP_011539091.1:p.Pro558His
XM_011540790.1:c.1583C>A	XP_011539092.1:p.Pro528His
XM_011540791.1:c.1583C>A	XP_011539093.1:p.Pro528His
XM_011540790.3:c.1583C>A	XP_011539092.1:p.Pro528His
XM_011540791.3:c.1583C>A	XP_011539093.1:p.Pro528His
XR_001736993.1:n.1663C>A
NM_144701.3:c.1583C>A MANE Select	NP_653302.2:p.Pro528His