Canonical Allele Identifier: CA418438815

Gene: IL23R

Linked Data

• dbSNP Id: rs1653095424
• gnomAD v3: 1-67258879-A-G
• gnomAD v4: 1-67258879-A-G
• MyVariant Identifiers: chr1:g.67724562A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258879A>G , CM000663.2:g.67258879A>G	GRCh38
NC_000001.10:g.67724562A>G , CM000663.1:g.67724562A>G	GRCh37
NC_000001.9:g.67497150A>G	NCBI36
NG_011498.1:g.97394A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1480A>G	ENSP00000513138.1:n.1480A>G
ENST00000697150.1:c.1538A>G	ENSP00000513139.1:n.1538A>G
ENST00000697151.1:c.1471A>G	ENSP00000513140.1:n.1471A>G
ENST00000697164.1:c.1551A>G	ENSP00000513153.1:p.Gly517=
ENST00000697165.1:c.1338A>G	ENSP00000513154.1:p.Gly446=
ENST00000347310.10:c.1641A>G MANE Select	ENSP00000321345.5:p.Gly547=
ENST00000637002.1:c.1032A>G	ENSP00000490340.1:p.Gly344=
ENST00000347310.9:c.1641A>G	ENSP00000321345.5:p.Gly547=
ENST00000395227.2:c.435A>G	ENSP00000378652.2:p.Gly145=
ENST00000425614.3:c.876A>G	ENSP00000387640.2:p.Gly292=
ENST00000473881.2:c.*467A>G	ENSP00000486667.1:n.*467A>G
NM_144701.2:c.1641A>G	NP_653302.2:p.Gly547=
XM_005270516.2:c.879A>G	XP_005270573.1:p.Gly293=
XM_011540789.1:c.1731A>G	XP_011539091.1:p.Gly577=
XM_011540790.1:c.1641A>G	XP_011539092.1:p.Gly547=
XM_011540791.1:c.1641A>G	XP_011539093.1:p.Gly547=
XM_011540790.3:c.1641A>G	XP_011539092.1:p.Gly547=
XM_011540791.3:c.1641A>G	XP_011539093.1:p.Gly547=
XR_001736993.1:n.1721A>G
NM_144701.3:c.1641A>G MANE Select	NP_653302.2:p.Gly547=