Canonical Allele Identifier: CA418438784

Gene: IL23R

Linked Data

• dbSNP Id: rs1653104315
• MyVariant Identifiers: chr1:g.67724739A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259056A>G , CM000663.2:g.67259056A>G	GRCh38
NC_000001.10:g.67724739A>G , CM000663.1:g.67724739A>G	GRCh37
NC_000001.9:g.67497327A>G	NCBI36
NG_011498.1:g.97571A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1657A>G	ENSP00000513138.1:n.1657A>G
ENST00000697150.1:c.1715A>G	ENSP00000513139.1:n.1715A>G
ENST00000697151.1:c.1648A>G	ENSP00000513140.1:n.1648A>G
ENST00000697164.1:c.1728A>G	ENSP00000513153.1:p.Pro576=
ENST00000697165.1:c.1515A>G	ENSP00000513154.1:p.Pro505=
ENST00000347310.10:c.1818A>G MANE Select	ENSP00000321345.5:p.Pro606=
ENST00000637002.1:c.1209A>G	ENSP00000490340.1:p.Pro403=
ENST00000347310.9:c.1818A>G	ENSP00000321345.5:p.Pro606=
ENST00000395227.2:c.612A>G	ENSP00000378652.2:p.Pro204=
ENST00000425614.3:c.1053A>G	ENSP00000387640.2:p.Pro351=
ENST00000473881.2:c.*644A>G	ENSP00000486667.1:n.*644A>G
NM_144701.2:c.1818A>G	NP_653302.2:p.Pro606=
XM_005270516.2:c.1056A>G	XP_005270573.1:p.Pro352=
XM_011540789.1:c.1908A>G	XP_011539091.1:p.Pro636=
XM_011540790.1:c.1818A>G	XP_011539092.1:p.Pro606=
XM_011540791.1:c.1818A>G	XP_011539093.1:p.Pro606=
XM_011540790.3:c.1818A>G	XP_011539092.1:p.Pro606=
XM_011540791.3:c.1818A>G	XP_011539093.1:p.Pro606=
XR_001736993.1:n.1898A>G
NM_144701.3:c.1818A>G MANE Select	NP_653302.2:p.Pro606=