Canonical Allele Identifier: CA340728749

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724495A>C (hg19) ; chr1:g.67258812A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258812A>C , CM000663.2:g.67258812A>C	GRCh38
NC_000001.10:g.67724495A>C , CM000663.1:g.67724495A>C	GRCh37
NC_000001.9:g.67497083A>C	NCBI36
NG_011498.1:g.97327A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1413A>C	ENSP00000513138.1:n.1413A>C
ENST00000697150.1:c.1471A>C	ENSP00000513139.1:n.1471A>C
ENST00000697151.1:c.1404A>C	ENSP00000513140.1:n.1404A>C
ENST00000697164.1:c.1484A>C	ENSP00000513153.1:p.Gln495Pro
ENST00000697165.1:c.1271A>C	ENSP00000513154.1:p.Gln424Pro
ENST00000347310.10:c.1574A>C MANE Select	ENSP00000321345.5:p.Gln525Pro
ENST00000637002.1:c.965A>C	ENSP00000490340.1:p.Gln322Pro
ENST00000347310.9:c.1574A>C	ENSP00000321345.5:p.Gln525Pro
ENST00000395227.2:c.368A>C	ENSP00000378652.2:p.Gln123Pro
ENST00000425614.3:c.809A>C	ENSP00000387640.2:p.Gln270Pro
ENST00000473881.2:c.*400A>C	ENSP00000486667.1:n.*400A>C
NM_144701.2:c.1574A>C	NP_653302.2:p.Gln525Pro
XM_005270516.2:c.812A>C	XP_005270573.1:p.Gln271Pro
XM_011540789.1:c.1664A>C	XP_011539091.1:p.Gln555Pro
XM_011540790.1:c.1574A>C	XP_011539092.1:p.Gln525Pro
XM_011540791.1:c.1574A>C	XP_011539093.1:p.Gln525Pro
XM_011540790.3:c.1574A>C	XP_011539092.1:p.Gln525Pro
XM_011540791.3:c.1574A>C	XP_011539093.1:p.Gln525Pro
XR_001736993.1:n.1654A>C
NM_144701.3:c.1574A>C MANE Select	NP_653302.2:p.Gln525Pro