Canonical Allele Identifier: CA340728728

Gene: IL23R

Linked Data

• gnomAD v4: 1-67258802-C-T
• COSMIC: COSM4468812
• MyVariant Identifiers: chr1:g.67724485C>T (hg19) ; chr1:g.67258802C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258802C>T , CM000663.2:g.67258802C>T	GRCh38
NC_000001.10:g.67724485C>T , CM000663.1:g.67724485C>T	GRCh37
NC_000001.9:g.67497073C>T	NCBI36
NG_011498.1:g.97317C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1403C>T	ENSP00000513138.1:n.1403C>T
ENST00000697150.1:c.1461C>T	ENSP00000513139.1:n.1461C>T
ENST00000697151.1:c.1394C>T	ENSP00000513140.1:n.1394C>T
ENST00000697164.1:c.1474C>T	ENSP00000513153.1:p.Pro492Ser
ENST00000697165.1:c.1261C>T	ENSP00000513154.1:p.Pro421Ser
ENST00000347310.10:c.1564C>T MANE Select	ENSP00000321345.5:p.Pro522Ser
ENST00000637002.1:c.955C>T	ENSP00000490340.1:p.Pro319Ser
ENST00000347310.9:c.1564C>T	ENSP00000321345.5:p.Pro522Ser
ENST00000395227.2:c.358C>T	ENSP00000378652.2:p.Pro120Ser
ENST00000425614.3:c.799C>T	ENSP00000387640.2:p.Pro267Ser
ENST00000473881.2:c.*390C>T	ENSP00000486667.1:n.*390C>T
NM_144701.2:c.1564C>T	NP_653302.2:p.Pro522Ser
XM_005270516.2:c.802C>T	XP_005270573.1:p.Pro268Ser
XM_011540789.1:c.1654C>T	XP_011539091.1:p.Pro552Ser
XM_011540790.1:c.1564C>T	XP_011539092.1:p.Pro522Ser
XM_011540791.1:c.1564C>T	XP_011539093.1:p.Pro522Ser
XM_011540790.3:c.1564C>T	XP_011539092.1:p.Pro522Ser
XM_011540791.3:c.1564C>T	XP_011539093.1:p.Pro522Ser
XR_001736993.1:n.1644C>T
NM_144701.3:c.1564C>T MANE Select	NP_653302.2:p.Pro522Ser