Canonical Allele Identifier: CA340729842

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259073T>C , CM000663.2:g.67259073T>C	GRCh38
NC_000001.10:g.67724756T>C , CM000663.1:g.67724756T>C	GRCh37
NC_000001.9:g.67497344T>C	NCBI36
NG_011498.1:g.97588T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_144701.3:c.1835T>C MANE Select	NP_653302.2:p.Phe612Ser
ENST00000347310.10:c.1835T>C MANE Select	ENSP00000321345.5:p.Phe612Ser
NM_144701.2:c.1835T>C	NP_653302.2:p.Phe612Ser
ENST00000347310.9:c.1835T>C	ENSP00000321345.5:p.Phe612Ser
ENST00000395227.2:c.629T>C	ENSP00000378652.2:p.Phe210Ser
ENST00000425614.3:c.1070T>C	ENSP00000387640.2:p.Phe357Ser
ENST00000473881.2:c.*661T>C	ENSP00000486667.1:n.*661T>C
ENST00000637002.1:c.1226T>C	ENSP00000490340.1:p.Phe409Ser
ENST00000697149.1:c.1674T>C	ENSP00000513138.1:n.1674T>C
ENST00000697150.1:c.1732T>C	ENSP00000513139.1:n.1732T>C
ENST00000697151.1:c.1665T>C	ENSP00000513140.1:n.1665T>C
ENST00000697164.1:c.1745T>C	ENSP00000513153.1:p.Phe582Ser
ENST00000697165.1:c.1532T>C	ENSP00000513154.1:p.Phe511Ser
XM_005270516.2:c.1073T>C	XP_005270573.1:p.Phe358Ser
XM_011540789.1:c.1925T>C	XP_011539091.1:p.Phe642Ser
XM_011540790.1:c.1835T>C	XP_011539092.1:p.Phe612Ser
XM_011540790.3:c.1835T>C	XP_011539092.1:p.Phe612Ser
XM_011540791.1:c.1835T>C	XP_011539093.1:p.Phe612Ser
XM_011540791.3:c.1835T>C	XP_011539093.1:p.Phe612Ser
XR_001736993.1:n.1915T>C