Canonical Allele Identifier: CA340729730

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724735T>C (hg19) ; chr1:g.67259052T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259052T>C , CM000663.2:g.67259052T>C	GRCh38
NC_000001.10:g.67724735T>C , CM000663.1:g.67724735T>C	GRCh37
NC_000001.9:g.67497323T>C	NCBI36
NG_011498.1:g.97567T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1653T>C	ENSP00000513138.1:n.1653T>C
ENST00000697150.1:c.1711T>C	ENSP00000513139.1:n.1711T>C
ENST00000697151.1:c.1644T>C	ENSP00000513140.1:n.1644T>C
ENST00000697164.1:c.1724T>C	ENSP00000513153.1:p.Leu575Ser
ENST00000697165.1:c.1511T>C	ENSP00000513154.1:p.Leu504Ser
ENST00000347310.10:c.1814T>C MANE Select	ENSP00000321345.5:p.Leu605Ser
ENST00000637002.1:c.1205T>C	ENSP00000490340.1:p.Leu402Ser
ENST00000347310.9:c.1814T>C	ENSP00000321345.5:p.Leu605Ser
ENST00000395227.2:c.608T>C	ENSP00000378652.2:p.Leu203Ser
ENST00000425614.3:c.1049T>C	ENSP00000387640.2:p.Leu350Ser
ENST00000473881.2:c.*640T>C	ENSP00000486667.1:n.*640T>C
NM_144701.2:c.1814T>C	NP_653302.2:p.Leu605Ser
XM_005270516.2:c.1052T>C	XP_005270573.1:p.Leu351Ser
XM_011540789.1:c.1904T>C	XP_011539091.1:p.Leu635Ser
XM_011540790.1:c.1814T>C	XP_011539092.1:p.Leu605Ser
XM_011540791.1:c.1814T>C	XP_011539093.1:p.Leu605Ser
XM_011540790.3:c.1814T>C	XP_011539092.1:p.Leu605Ser
XM_011540791.3:c.1814T>C	XP_011539093.1:p.Leu605Ser
XR_001736993.1:n.1894T>C
NM_144701.3:c.1814T>C MANE Select	NP_653302.2:p.Leu605Ser