Canonical Allele Identifier: CA340730150

Gene: IL23R

Linked Data

• gnomAD v4: 1-67259118-T-C
• MyVariant Identifiers: chr1:g.67724801T>C (hg19) ; chr1:g.67259118T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259118T>C , CM000663.2:g.67259118T>C	GRCh38
NC_000001.10:g.67724801T>C , CM000663.1:g.67724801T>C	GRCh37
NC_000001.9:g.67497389T>C	NCBI36
NG_011498.1:g.97633T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1719T>C	ENSP00000513138.1:n.1719T>C
ENST00000697150.1:c.1777T>C	ENSP00000513139.1:n.1777T>C
ENST00000697151.1:c.1710T>C	ENSP00000513140.1:n.1710T>C
ENST00000697164.1:c.1790T>C	ENSP00000513153.1:p.Leu597Ser
ENST00000697165.1:c.1577T>C	ENSP00000513154.1:p.Leu526Ser
ENST00000347310.10:c.1880T>C MANE Select	ENSP00000321345.5:p.Leu627Ser
ENST00000637002.1:c.1271T>C	ENSP00000490340.1:p.Leu424Ser
ENST00000347310.9:c.1880T>C	ENSP00000321345.5:p.Leu627Ser
ENST00000395227.2:c.674T>C	ENSP00000378652.2:p.Leu225Ser
ENST00000425614.3:c.1115T>C	ENSP00000387640.2:p.Leu372Ser
ENST00000473881.2:c.*706T>C	ENSP00000486667.1:n.*706T>C
NM_144701.2:c.1880T>C	NP_653302.2:p.Leu627Ser
XM_005270516.2:c.1118T>C	XP_005270573.1:p.Leu373Ser
XM_011540789.1:c.1970T>C	XP_011539091.1:p.Leu657Ser
XM_011540790.1:c.1880T>C	XP_011539092.1:p.Leu627Ser
XM_011540791.1:c.1880T>C	XP_011539093.1:p.Leu627Ser
XM_011540790.3:c.1880T>C	XP_011539092.1:p.Leu627Ser
XM_011540791.3:c.1880T>C	XP_011539093.1:p.Leu627Ser
XR_001736993.1:n.1960T>C
NM_144701.3:c.1880T>C MANE Select	NP_653302.2:p.Leu627Ser