Canonical Allele Identifier: CA340730027

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724785A>C (hg19) ; chr1:g.67259102A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259102A>C , CM000663.2:g.67259102A>C	GRCh38
NC_000001.10:g.67724785A>C , CM000663.1:g.67724785A>C	GRCh37
NC_000001.9:g.67497373A>C	NCBI36
NG_011498.1:g.97617A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1703A>C	ENSP00000513138.1:n.1703A>C
ENST00000697150.1:c.1761A>C	ENSP00000513139.1:n.1761A>C
ENST00000697151.1:c.1694A>C	ENSP00000513140.1:n.1694A>C
ENST00000697164.1:c.1774A>C	ENSP00000513153.1:p.Asn592His
ENST00000697165.1:c.1561A>C	ENSP00000513154.1:p.Asn521His
ENST00000347310.10:c.1864A>C MANE Select	ENSP00000321345.5:p.Asn622His
ENST00000637002.1:c.1255A>C	ENSP00000490340.1:p.Asn419His
ENST00000347310.9:c.1864A>C	ENSP00000321345.5:p.Asn622His
ENST00000395227.2:c.658A>C	ENSP00000378652.2:p.Asn220His
ENST00000425614.3:c.1099A>C	ENSP00000387640.2:p.Asn367His
ENST00000473881.2:c.*690A>C	ENSP00000486667.1:n.*690A>C
NM_144701.2:c.1864A>C	NP_653302.2:p.Asn622His
XM_005270516.2:c.1102A>C	XP_005270573.1:p.Asn368His
XM_011540789.1:c.1954A>C	XP_011539091.1:p.Asn652His
XM_011540790.1:c.1864A>C	XP_011539092.1:p.Asn622His
XM_011540791.1:c.1864A>C	XP_011539093.1:p.Asn622His
XM_011540790.3:c.1864A>C	XP_011539092.1:p.Asn622His
XM_011540791.3:c.1864A>C	XP_011539093.1:p.Asn622His
XR_001736993.1:n.1944A>C
NM_144701.3:c.1864A>C MANE Select	NP_653302.2:p.Asn622His