Canonical Allele Identifier: CA418438795

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724547C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258864C>T , CM000663.2:g.67258864C>T	GRCh38
NC_000001.10:g.67724547C>T , CM000663.1:g.67724547C>T	GRCh37
NC_000001.9:g.67497135C>T	NCBI36
NG_011498.1:g.97379C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1465C>T	ENSP00000513138.1:n.1465C>T
ENST00000697150.1:c.1523C>T	ENSP00000513139.1:n.1523C>T
ENST00000697151.1:c.1456C>T	ENSP00000513140.1:n.1456C>T
ENST00000697164.1:c.1536C>T	ENSP00000513153.1:p.Asn512=
ENST00000697165.1:c.1323C>T	ENSP00000513154.1:p.Asn441=
ENST00000347310.10:c.1626C>T MANE Select	ENSP00000321345.5:p.Asn542=
ENST00000637002.1:c.1017C>T	ENSP00000490340.1:p.Asn339=
ENST00000347310.9:c.1626C>T	ENSP00000321345.5:p.Asn542=
ENST00000395227.2:c.420C>T	ENSP00000378652.2:p.Asn140=
ENST00000425614.3:c.861C>T	ENSP00000387640.2:p.Asn287=
ENST00000473881.2:c.*452C>T	ENSP00000486667.1:n.*452C>T
NM_144701.2:c.1626C>T	NP_653302.2:p.Asn542=
XM_005270516.2:c.864C>T	XP_005270573.1:p.Asn288=
XM_011540789.1:c.1716C>T	XP_011539091.1:p.Asn572=
XM_011540790.1:c.1626C>T	XP_011539092.1:p.Asn542=
XM_011540791.1:c.1626C>T	XP_011539093.1:p.Asn542=
XM_011540790.3:c.1626C>T	XP_011539092.1:p.Asn542=
XM_011540791.3:c.1626C>T	XP_011539093.1:p.Asn542=
XR_001736993.1:n.1706C>T
NM_144701.3:c.1626C>T MANE Select	NP_653302.2:p.Asn542=