Canonical Allele Identifier: CA340729228

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724605G>C (hg19) ; chr1:g.67258922G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258922G>C , CM000663.2:g.67258922G>C	GRCh38
NC_000001.10:g.67724605G>C , CM000663.1:g.67724605G>C	GRCh37
NC_000001.9:g.67497193G>C	NCBI36
NG_011498.1:g.97437G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1523G>C	ENSP00000513138.1:n.1523G>C
ENST00000697150.1:c.1581G>C	ENSP00000513139.1:n.1581G>C
ENST00000697151.1:c.1514G>C	ENSP00000513140.1:n.1514G>C
ENST00000697164.1:c.1594G>C	ENSP00000513153.1:p.Asp532His
ENST00000697165.1:c.1381G>C	ENSP00000513154.1:p.Asp461His
ENST00000347310.10:c.1684G>C MANE Select	ENSP00000321345.5:p.Asp562His
ENST00000637002.1:c.1075G>C	ENSP00000490340.1:p.Asp359His
ENST00000347310.9:c.1684G>C	ENSP00000321345.5:p.Asp562His
ENST00000395227.2:c.478G>C	ENSP00000378652.2:p.Asp160His
ENST00000425614.3:c.919G>C	ENSP00000387640.2:p.Asp307His
ENST00000473881.2:c.*510G>C	ENSP00000486667.1:n.*510G>C
NM_144701.2:c.1684G>C	NP_653302.2:p.Asp562His
XM_005270516.2:c.922G>C	XP_005270573.1:p.Asp308His
XM_011540789.1:c.1774G>C	XP_011539091.1:p.Asp592His
XM_011540790.1:c.1684G>C	XP_011539092.1:p.Asp562His
XM_011540791.1:c.1684G>C	XP_011539093.1:p.Asp562His
XM_011540790.3:c.1684G>C	XP_011539092.1:p.Asp562His
XM_011540791.3:c.1684G>C	XP_011539093.1:p.Asp562His
XR_001736993.1:n.1764G>C
NM_144701.3:c.1684G>C MANE Select	NP_653302.2:p.Asp562His