Canonical Allele Identifier: CA340729371

Gene: IL23R

Linked Data

• gnomAD v4: 1-67258953-C-G
• MyVariant Identifiers: chr1:g.67724636C>G (hg19) ; chr1:g.67258953C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258953C>G , CM000663.2:g.67258953C>G	GRCh38
NC_000001.10:g.67724636C>G , CM000663.1:g.67724636C>G	GRCh37
NC_000001.9:g.67497224C>G	NCBI36
NG_011498.1:g.97468C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1554C>G	ENSP00000513138.1:n.1554C>G
ENST00000697150.1:c.1612C>G	ENSP00000513139.1:n.1612C>G
ENST00000697151.1:c.1545C>G	ENSP00000513140.1:n.1545C>G
ENST00000697164.1:c.1625C>G	ENSP00000513153.1:p.Thr542Ser
ENST00000697165.1:c.1412C>G	ENSP00000513154.1:p.Thr471Ser
ENST00000347310.10:c.1715C>G MANE Select	ENSP00000321345.5:p.Thr572Ser
ENST00000637002.1:c.1106C>G	ENSP00000490340.1:p.Thr369Ser
ENST00000347310.9:c.1715C>G	ENSP00000321345.5:p.Thr572Ser
ENST00000395227.2:c.509C>G	ENSP00000378652.2:p.Thr170Ser
ENST00000425614.3:c.950C>G	ENSP00000387640.2:p.Thr317Ser
ENST00000473881.2:c.*541C>G	ENSP00000486667.1:n.*541C>G
NM_144701.2:c.1715C>G	NP_653302.2:p.Thr572Ser
XM_005270516.2:c.953C>G	XP_005270573.1:p.Thr318Ser
XM_011540789.1:c.1805C>G	XP_011539091.1:p.Thr602Ser
XM_011540790.1:c.1715C>G	XP_011539092.1:p.Thr572Ser
XM_011540791.1:c.1715C>G	XP_011539093.1:p.Thr572Ser
XM_011540790.3:c.1715C>G	XP_011539092.1:p.Thr572Ser
XM_011540791.3:c.1715C>G	XP_011539093.1:p.Thr572Ser
XR_001736993.1:n.1795C>G
NM_144701.3:c.1715C>G MANE Select	NP_653302.2:p.Thr572Ser