Canonical Allele Identifier: CA340730016

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259100T>C , CM000663.2:g.67259100T>C	GRCh38
NC_000001.10:g.67724783T>C , CM000663.1:g.67724783T>C	GRCh37
NC_000001.9:g.67497371T>C	NCBI36
NG_011498.1:g.97615T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_144701.3:c.1862T>C MANE Select	NP_653302.2:p.Phe621Ser
ENST00000347310.10:c.1862T>C MANE Select	ENSP00000321345.5:p.Phe621Ser
NM_144701.2:c.1862T>C	NP_653302.2:p.Phe621Ser
ENST00000347310.9:c.1862T>C	ENSP00000321345.5:p.Phe621Ser
ENST00000395227.2:c.656T>C	ENSP00000378652.2:p.Phe219Ser
ENST00000425614.3:c.1097T>C	ENSP00000387640.2:p.Phe366Ser
ENST00000473881.2:c.*688T>C	ENSP00000486667.1:n.*688T>C
ENST00000637002.1:c.1253T>C	ENSP00000490340.1:p.Phe418Ser
ENST00000697149.1:c.1701T>C	ENSP00000513138.1:n.1701T>C
ENST00000697150.1:c.1759T>C	ENSP00000513139.1:n.1759T>C
ENST00000697151.1:c.1692T>C	ENSP00000513140.1:n.1692T>C
ENST00000697164.1:c.1772T>C	ENSP00000513153.1:p.Phe591Ser
ENST00000697165.1:c.1559T>C	ENSP00000513154.1:p.Phe520Ser
XM_005270516.2:c.1100T>C	XP_005270573.1:p.Phe367Ser
XM_011540789.1:c.1952T>C	XP_011539091.1:p.Phe651Ser
XM_011540790.1:c.1862T>C	XP_011539092.1:p.Phe621Ser
XM_011540790.3:c.1862T>C	XP_011539092.1:p.Phe621Ser
XM_011540791.1:c.1862T>C	XP_011539093.1:p.Phe621Ser
XM_011540791.3:c.1862T>C	XP_011539093.1:p.Phe621Ser
XR_001736993.1:n.1942T>C