Canonical Allele Identifier: CA418438734

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259014T>C , CM000663.2:g.67259014T>C	GRCh38
NC_000001.10:g.67724697T>C , CM000663.1:g.67724697T>C	GRCh37
NC_000001.9:g.67497285T>C	NCBI36
NG_011498.1:g.97529T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_144701.3:c.1776T>C MANE Select	NP_653302.2:p.Asp592=
ENST00000347310.10:c.1776T>C MANE Select	ENSP00000321345.5:p.Asp592=
NM_144701.2:c.1776T>C	NP_653302.2:p.Asp592=
ENST00000347310.9:c.1776T>C	ENSP00000321345.5:p.Asp592=
ENST00000395227.2:c.570T>C	ENSP00000378652.2:p.Asp190=
ENST00000425614.3:c.1011T>C	ENSP00000387640.2:p.Asp337=
ENST00000473881.2:c.*602T>C	ENSP00000486667.1:n.*602T>C
ENST00000637002.1:c.1167T>C	ENSP00000490340.1:p.Asp389=
ENST00000697149.1:c.1615T>C	ENSP00000513138.1:n.1615T>C
ENST00000697150.1:c.1673T>C	ENSP00000513139.1:n.1673T>C
ENST00000697151.1:c.1606T>C	ENSP00000513140.1:n.1606T>C
ENST00000697164.1:c.1686T>C	ENSP00000513153.1:p.Asp562=
ENST00000697165.1:c.1473T>C	ENSP00000513154.1:p.Asp491=
XM_005270516.2:c.1014T>C	XP_005270573.1:p.Asp338=
XM_011540789.1:c.1866T>C	XP_011539091.1:p.Asp622=
XM_011540790.1:c.1776T>C	XP_011539092.1:p.Asp592=
XM_011540790.3:c.1776T>C	XP_011539092.1:p.Asp592=
XM_011540791.1:c.1776T>C	XP_011539093.1:p.Asp592=
XM_011540791.3:c.1776T>C	XP_011539093.1:p.Asp592=
XR_001736993.1:n.1856T>C