Canonical Allele Identifier: CA340729833

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724755T>C (hg19) ; chr1:g.67259072T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259072T>C , CM000663.2:g.67259072T>C	GRCh38
NC_000001.10:g.67724755T>C , CM000663.1:g.67724755T>C	GRCh37
NC_000001.9:g.67497343T>C	NCBI36
NG_011498.1:g.97587T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1673T>C	ENSP00000513138.1:n.1673T>C
ENST00000697150.1:c.1731T>C	ENSP00000513139.1:n.1731T>C
ENST00000697151.1:c.1664T>C	ENSP00000513140.1:n.1664T>C
ENST00000697164.1:c.1744T>C	ENSP00000513153.1:p.Phe582Leu
ENST00000697165.1:c.1531T>C	ENSP00000513154.1:p.Phe511Leu
ENST00000347310.10:c.1834T>C MANE Select	ENSP00000321345.5:p.Phe612Leu
ENST00000637002.1:c.1225T>C	ENSP00000490340.1:p.Phe409Leu
ENST00000347310.9:c.1834T>C	ENSP00000321345.5:p.Phe612Leu
ENST00000395227.2:c.628T>C	ENSP00000378652.2:p.Phe210Leu
ENST00000425614.3:c.1069T>C	ENSP00000387640.2:p.Phe357Leu
ENST00000473881.2:c.*660T>C	ENSP00000486667.1:n.*660T>C
NM_144701.2:c.1834T>C	NP_653302.2:p.Phe612Leu
XM_005270516.2:c.1072T>C	XP_005270573.1:p.Phe358Leu
XM_011540789.1:c.1924T>C	XP_011539091.1:p.Phe642Leu
XM_011540790.1:c.1834T>C	XP_011539092.1:p.Phe612Leu
XM_011540791.1:c.1834T>C	XP_011539093.1:p.Phe612Leu
XM_011540790.3:c.1834T>C	XP_011539092.1:p.Phe612Leu
XM_011540791.3:c.1834T>C	XP_011539093.1:p.Phe612Leu
XR_001736993.1:n.1914T>C
NM_144701.3:c.1834T>C MANE Select	NP_653302.2:p.Phe612Leu