Canonical Allele Identifier: CA418438620

Gene: IL23R

Linked Data

• dbSNP Id: rs1484077663
• gnomAD v2: 1-67724607-C-T
• MyVariant Identifiers: chr1:g.67724607C>T (hg19) ; chr1:g.67258924C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258924C>T , CM000663.2:g.67258924C>T	GRCh38
NC_000001.10:g.67724607C>T , CM000663.1:g.67724607C>T	GRCh37
NC_000001.9:g.67497195C>T	NCBI36
NG_011498.1:g.97439C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1525C>T	ENSP00000513138.1:n.1525C>T
ENST00000697150.1:c.1583C>T	ENSP00000513139.1:n.1583C>T
ENST00000697151.1:c.1516C>T	ENSP00000513140.1:n.1516C>T
ENST00000697164.1:c.1596C>T	ENSP00000513153.1:p.Asp532=
ENST00000697165.1:c.1383C>T	ENSP00000513154.1:p.Asp461=
ENST00000347310.10:c.1686C>T MANE Select	ENSP00000321345.5:p.Asp562=
ENST00000637002.1:c.1077C>T	ENSP00000490340.1:p.Asp359=
ENST00000347310.9:c.1686C>T	ENSP00000321345.5:p.Asp562=
ENST00000395227.2:c.480C>T	ENSP00000378652.2:p.Asp160=
ENST00000425614.3:c.921C>T	ENSP00000387640.2:p.Asp307=
ENST00000473881.2:c.*512C>T	ENSP00000486667.1:n.*512C>T
NM_144701.2:c.1686C>T	NP_653302.2:p.Asp562=
XM_005270516.2:c.924C>T	XP_005270573.1:p.Asp308=
XM_011540789.1:c.1776C>T	XP_011539091.1:p.Asp592=
XM_011540790.1:c.1686C>T	XP_011539092.1:p.Asp562=
XM_011540791.1:c.1686C>T	XP_011539093.1:p.Asp562=
XM_011540790.3:c.1686C>T	XP_011539092.1:p.Asp562=
XM_011540791.3:c.1686C>T	XP_011539093.1:p.Asp562=
XR_001736993.1:n.1766C>T
NM_144701.3:c.1686C>T MANE Select	NP_653302.2:p.Asp562=