Canonical Allele Identifier: CA340729352

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724632A>C (hg19) ; chr1:g.67258949A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258949A>C , CM000663.2:g.67258949A>C	GRCh38
NC_000001.10:g.67724632A>C , CM000663.1:g.67724632A>C	GRCh37
NC_000001.9:g.67497220A>C	NCBI36
NG_011498.1:g.97464A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1550A>C	ENSP00000513138.1:n.1550A>C
ENST00000697150.1:c.1608A>C	ENSP00000513139.1:n.1608A>C
ENST00000697151.1:c.1541A>C	ENSP00000513140.1:n.1541A>C
ENST00000697164.1:c.1621A>C	ENSP00000513153.1:p.Thr541Pro
ENST00000697165.1:c.1408A>C	ENSP00000513154.1:p.Thr470Pro
ENST00000347310.10:c.1711A>C MANE Select	ENSP00000321345.5:p.Thr571Pro
ENST00000637002.1:c.1102A>C	ENSP00000490340.1:p.Thr368Pro
ENST00000347310.9:c.1711A>C	ENSP00000321345.5:p.Thr571Pro
ENST00000395227.2:c.505A>C	ENSP00000378652.2:p.Thr169Pro
ENST00000425614.3:c.946A>C	ENSP00000387640.2:p.Thr316Pro
ENST00000473881.2:c.*537A>C	ENSP00000486667.1:n.*537A>C
NM_144701.2:c.1711A>C	NP_653302.2:p.Thr571Pro
XM_005270516.2:c.949A>C	XP_005270573.1:p.Thr317Pro
XM_011540789.1:c.1801A>C	XP_011539091.1:p.Thr601Pro
XM_011540790.1:c.1711A>C	XP_011539092.1:p.Thr571Pro
XM_011540791.1:c.1711A>C	XP_011539093.1:p.Thr571Pro
XM_011540790.3:c.1711A>C	XP_011539092.1:p.Thr571Pro
XM_011540791.3:c.1711A>C	XP_011539093.1:p.Thr571Pro
XR_001736993.1:n.1791A>C
NM_144701.3:c.1711A>C MANE Select	NP_653302.2:p.Thr571Pro