Canonical Allele Identifier: CA340729473

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724665G>C (hg19) ; chr1:g.67258982G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258982G>C , CM000663.2:g.67258982G>C	GRCh38
NC_000001.10:g.67724665G>C , CM000663.1:g.67724665G>C	GRCh37
NC_000001.9:g.67497253G>C	NCBI36
NG_011498.1:g.97497G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1583G>C	ENSP00000513138.1:n.1583G>C
ENST00000697150.1:c.1641G>C	ENSP00000513139.1:n.1641G>C
ENST00000697151.1:c.1574G>C	ENSP00000513140.1:n.1574G>C
ENST00000697164.1:c.1654G>C	ENSP00000513153.1:p.Glu552Gln
ENST00000697165.1:c.1441G>C	ENSP00000513154.1:p.Glu481Gln
ENST00000347310.10:c.1744G>C MANE Select	ENSP00000321345.5:p.Glu582Gln
ENST00000637002.1:c.1135G>C	ENSP00000490340.1:p.Glu379Gln
ENST00000347310.9:c.1744G>C	ENSP00000321345.5:p.Glu582Gln
ENST00000395227.2:c.538G>C	ENSP00000378652.2:p.Glu180Gln
ENST00000425614.3:c.979G>C	ENSP00000387640.2:p.Glu327Gln
ENST00000473881.2:c.*570G>C	ENSP00000486667.1:n.*570G>C
NM_144701.2:c.1744G>C	NP_653302.2:p.Glu582Gln
XM_005270516.2:c.982G>C	XP_005270573.1:p.Glu328Gln
XM_011540789.1:c.1834G>C	XP_011539091.1:p.Glu612Gln
XM_011540790.1:c.1744G>C	XP_011539092.1:p.Glu582Gln
XM_011540791.1:c.1744G>C	XP_011539093.1:p.Glu582Gln
XM_011540790.3:c.1744G>C	XP_011539092.1:p.Glu582Gln
XM_011540791.3:c.1744G>C	XP_011539093.1:p.Glu582Gln
XR_001736993.1:n.1824G>C
NM_144701.3:c.1744G>C MANE Select	NP_653302.2:p.Glu582Gln