Canonical Allele Identifier: CA418438747

Gene: IL23R

Linked Data

• gnomAD v4: 1-67259026-C-T
• MyVariant Identifiers: chr1:g.67724709C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259026C>T , CM000663.2:g.67259026C>T	GRCh38
NC_000001.10:g.67724709C>T , CM000663.1:g.67724709C>T	GRCh37
NC_000001.9:g.67497297C>T	NCBI36
NG_011498.1:g.97541C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1627C>T	ENSP00000513138.1:n.1627C>T
ENST00000697150.1:c.1685C>T	ENSP00000513139.1:n.1685C>T
ENST00000697151.1:c.1618C>T	ENSP00000513140.1:n.1618C>T
ENST00000697164.1:c.1698C>T	ENSP00000513153.1:p.Ser566=
ENST00000697165.1:c.1485C>T	ENSP00000513154.1:p.Ser495=
ENST00000347310.10:c.1788C>T MANE Select	ENSP00000321345.5:p.Ser596=
ENST00000637002.1:c.1179C>T	ENSP00000490340.1:p.Ser393=
ENST00000347310.9:c.1788C>T	ENSP00000321345.5:p.Ser596=
ENST00000395227.2:c.582C>T	ENSP00000378652.2:p.Ser194=
ENST00000425614.3:c.1023C>T	ENSP00000387640.2:p.Ser341=
ENST00000473881.2:c.*614C>T	ENSP00000486667.1:n.*614C>T
NM_144701.2:c.1788C>T	NP_653302.2:p.Ser596=
XM_005270516.2:c.1026C>T	XP_005270573.1:p.Ser342=
XM_011540789.1:c.1878C>T	XP_011539091.1:p.Ser626=
XM_011540790.1:c.1788C>T	XP_011539092.1:p.Ser596=
XM_011540791.1:c.1788C>T	XP_011539093.1:p.Ser596=
XM_011540790.3:c.1788C>T	XP_011539092.1:p.Ser596=
XM_011540791.3:c.1788C>T	XP_011539093.1:p.Ser596=
XR_001736993.1:n.1868C>T
NM_144701.3:c.1788C>T MANE Select	NP_653302.2:p.Ser596=