Canonical Allele Identifier: CA340728622

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724435C>A (hg19) ; chr1:g.67258752C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258752C>A , CM000663.2:g.67258752C>A	GRCh38
NC_000001.10:g.67724435C>A , CM000663.1:g.67724435C>A	GRCh37
NC_000001.9:g.67497023C>A	NCBI36
NG_011498.1:g.97267C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1353C>A	ENSP00000513138.1:n.1353C>A
ENST00000697150.1:c.1411C>A	ENSP00000513139.1:n.1411C>A
ENST00000697151.1:c.1344C>A	ENSP00000513140.1:n.1344C>A
ENST00000697164.1:c.1424C>A	ENSP00000513153.1:p.Thr475Asn
ENST00000697165.1:c.1211C>A	ENSP00000513154.1:p.Thr404Asn
ENST00000347310.10:c.1514C>A MANE Select	ENSP00000321345.5:p.Thr505Asn
ENST00000637002.1:c.905C>A	ENSP00000490340.1:p.Thr302Asn
ENST00000347310.9:c.1514C>A	ENSP00000321345.5:p.Thr505Asn
ENST00000395227.2:c.308C>A	ENSP00000378652.2:p.Thr103Asn
ENST00000425614.3:c.749C>A	ENSP00000387640.2:p.Thr250Asn
ENST00000473881.2:c.*340C>A	ENSP00000486667.1:n.*340C>A
NM_144701.2:c.1514C>A	NP_653302.2:p.Thr505Asn
XM_005270516.2:c.752C>A	XP_005270573.1:p.Thr251Asn
XM_011540789.1:c.1604C>A	XP_011539091.1:p.Thr535Asn
XM_011540790.1:c.1514C>A	XP_011539092.1:p.Thr505Asn
XM_011540791.1:c.1514C>A	XP_011539093.1:p.Thr505Asn
XM_011540790.3:c.1514C>A	XP_011539092.1:p.Thr505Asn
XM_011540791.3:c.1514C>A	XP_011539093.1:p.Thr505Asn
XR_001736993.1:n.1594C>A
NM_144701.3:c.1514C>A MANE Select	NP_653302.2:p.Thr505Asn