Canonical Allele Identifier: CA340728778

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724507A>G (hg19) ; chr1:g.67258824A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258824A>G , CM000663.2:g.67258824A>G	GRCh38
NC_000001.10:g.67724507A>G , CM000663.1:g.67724507A>G	GRCh37
NC_000001.9:g.67497095A>G	NCBI36
NG_011498.1:g.97339A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1425A>G	ENSP00000513138.1:n.1425A>G
ENST00000697150.1:c.1483A>G	ENSP00000513139.1:n.1483A>G
ENST00000697151.1:c.1416A>G	ENSP00000513140.1:n.1416A>G
ENST00000697164.1:c.1496A>G	ENSP00000513153.1:p.Asn499Ser
ENST00000697165.1:c.1283A>G	ENSP00000513154.1:p.Asn428Ser
ENST00000347310.10:c.1586A>G MANE Select	ENSP00000321345.5:p.Asn529Ser
ENST00000637002.1:c.977A>G	ENSP00000490340.1:p.Asn326Ser
ENST00000347310.9:c.1586A>G	ENSP00000321345.5:p.Asn529Ser
ENST00000395227.2:c.380A>G	ENSP00000378652.2:p.Asn127Ser
ENST00000425614.3:c.821A>G	ENSP00000387640.2:p.Asn274Ser
ENST00000473881.2:c.*412A>G	ENSP00000486667.1:n.*412A>G
NM_144701.2:c.1586A>G	NP_653302.2:p.Asn529Ser
XM_005270516.2:c.824A>G	XP_005270573.1:p.Asn275Ser
XM_011540789.1:c.1676A>G	XP_011539091.1:p.Asn559Ser
XM_011540790.1:c.1586A>G	XP_011539092.1:p.Asn529Ser
XM_011540791.1:c.1586A>G	XP_011539093.1:p.Asn529Ser
XM_011540790.3:c.1586A>G	XP_011539092.1:p.Asn529Ser
XM_011540791.3:c.1586A>G	XP_011539093.1:p.Asn529Ser
XR_001736993.1:n.1666A>G
NM_144701.3:c.1586A>G MANE Select	NP_653302.2:p.Asn529Ser