Canonical Allele Identifier: CA340729448

Gene: IL23R

Linked Data

• dbSNP Id: rs1653099467
• gnomAD v3: 1-67258976-C-T
• gnomAD v4: 1-67258976-C-T
• MyVariant Identifiers: chr1:g.67724659C>T (hg19) ; chr1:g.67258976C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258976C>T , CM000663.2:g.67258976C>T	GRCh38
NC_000001.10:g.67724659C>T , CM000663.1:g.67724659C>T	GRCh37
NC_000001.9:g.67497247C>T	NCBI36
NG_011498.1:g.97491C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1577C>T	ENSP00000513138.1:n.1577C>T
ENST00000697150.1:c.1635C>T	ENSP00000513139.1:n.1635C>T
ENST00000697151.1:c.1568C>T	ENSP00000513140.1:n.1568C>T
ENST00000697164.1:c.1648C>T	ENSP00000513153.1:p.Pro550Ser
ENST00000697165.1:c.1435C>T	ENSP00000513154.1:p.Pro479Ser
ENST00000347310.10:c.1738C>T MANE Select	ENSP00000321345.5:p.Pro580Ser
ENST00000637002.1:c.1129C>T	ENSP00000490340.1:p.Pro377Ser
ENST00000347310.9:c.1738C>T	ENSP00000321345.5:p.Pro580Ser
ENST00000395227.2:c.532C>T	ENSP00000378652.2:p.Pro178Ser
ENST00000425614.3:c.973C>T	ENSP00000387640.2:p.Pro325Ser
ENST00000473881.2:c.*564C>T	ENSP00000486667.1:n.*564C>T
NM_144701.2:c.1738C>T	NP_653302.2:p.Pro580Ser
XM_005270516.2:c.976C>T	XP_005270573.1:p.Pro326Ser
XM_011540789.1:c.1828C>T	XP_011539091.1:p.Pro610Ser
XM_011540790.1:c.1738C>T	XP_011539092.1:p.Pro580Ser
XM_011540791.1:c.1738C>T	XP_011539093.1:p.Pro580Ser
XM_011540790.3:c.1738C>T	XP_011539092.1:p.Pro580Ser
XM_011540791.3:c.1738C>T	XP_011539093.1:p.Pro580Ser
XR_001736993.1:n.1818C>T
NM_144701.3:c.1738C>T MANE Select	NP_653302.2:p.Pro580Ser