Canonical Allele Identifier: CA340729740

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724737C>T (hg19) ; chr1:g.67259054C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259054C>T , CM000663.2:g.67259054C>T	GRCh38
NC_000001.10:g.67724737C>T , CM000663.1:g.67724737C>T	GRCh37
NC_000001.9:g.67497325C>T	NCBI36
NG_011498.1:g.97569C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1655C>T	ENSP00000513138.1:n.1655C>T
ENST00000697150.1:c.1713C>T	ENSP00000513139.1:n.1713C>T
ENST00000697151.1:c.1646C>T	ENSP00000513140.1:n.1646C>T
ENST00000697164.1:c.1726C>T	ENSP00000513153.1:p.Pro576Ser
ENST00000697165.1:c.1513C>T	ENSP00000513154.1:p.Pro505Ser
ENST00000347310.10:c.1816C>T MANE Select	ENSP00000321345.5:p.Pro606Ser
ENST00000637002.1:c.1207C>T	ENSP00000490340.1:p.Pro403Ser
ENST00000347310.9:c.1816C>T	ENSP00000321345.5:p.Pro606Ser
ENST00000395227.2:c.610C>T	ENSP00000378652.2:p.Pro204Ser
ENST00000425614.3:c.1051C>T	ENSP00000387640.2:p.Pro351Ser
ENST00000473881.2:c.*642C>T	ENSP00000486667.1:n.*642C>T
NM_144701.2:c.1816C>T	NP_653302.2:p.Pro606Ser
XM_005270516.2:c.1054C>T	XP_005270573.1:p.Pro352Ser
XM_011540789.1:c.1906C>T	XP_011539091.1:p.Pro636Ser
XM_011540790.1:c.1816C>T	XP_011539092.1:p.Pro606Ser
XM_011540791.1:c.1816C>T	XP_011539093.1:p.Pro606Ser
XM_011540790.3:c.1816C>T	XP_011539092.1:p.Pro606Ser
XM_011540791.3:c.1816C>T	XP_011539093.1:p.Pro606Ser
XR_001736993.1:n.1896C>T
NM_144701.3:c.1816C>T MANE Select	NP_653302.2:p.Pro606Ser