Canonical Allele Identifier: CA418438663

Gene: IL23R

Linked Data

• dbSNP Id: rs2100397935
• gnomAD v4: 1-67258762-A-G
• MyVariant Identifiers: chr1:g.67724445A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258762A>G , CM000663.2:g.67258762A>G	GRCh38
NC_000001.10:g.67724445A>G , CM000663.1:g.67724445A>G	GRCh37
NC_000001.9:g.67497033A>G	NCBI36
NG_011498.1:g.97277A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1363A>G	ENSP00000513138.1:n.1363A>G
ENST00000697150.1:c.1421A>G	ENSP00000513139.1:n.1421A>G
ENST00000697151.1:c.1354A>G	ENSP00000513140.1:n.1354A>G
ENST00000697164.1:c.1434A>G	ENSP00000513153.1:p.Thr478=
ENST00000697165.1:c.1221A>G	ENSP00000513154.1:p.Thr407=
ENST00000347310.10:c.1524A>G MANE Select	ENSP00000321345.5:p.Thr508=
ENST00000637002.1:c.915A>G	ENSP00000490340.1:p.Thr305=
ENST00000347310.9:c.1524A>G	ENSP00000321345.5:p.Thr508=
ENST00000395227.2:c.318A>G	ENSP00000378652.2:p.Thr106=
ENST00000425614.3:c.759A>G	ENSP00000387640.2:p.Thr253=
ENST00000473881.2:c.*350A>G	ENSP00000486667.1:n.*350A>G
NM_144701.2:c.1524A>G	NP_653302.2:p.Thr508=
XM_005270516.2:c.762A>G	XP_005270573.1:p.Thr254=
XM_011540789.1:c.1614A>G	XP_011539091.1:p.Thr538=
XM_011540790.1:c.1524A>G	XP_011539092.1:p.Thr508=
XM_011540791.1:c.1524A>G	XP_011539093.1:p.Thr508=
XM_011540790.3:c.1524A>G	XP_011539092.1:p.Thr508=
XM_011540791.3:c.1524A>G	XP_011539093.1:p.Thr508=
XR_001736993.1:n.1604A>G
NM_144701.3:c.1524A>G MANE Select	NP_653302.2:p.Thr508=