Canonical Allele Identifier: CA340728843

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724531T>C (hg19) ; chr1:g.67258848T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258848T>C , CM000663.2:g.67258848T>C	GRCh38
NC_000001.10:g.67724531T>C , CM000663.1:g.67724531T>C	GRCh37
NC_000001.9:g.67497119T>C	NCBI36
NG_011498.1:g.97363T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1449T>C	ENSP00000513138.1:n.1449T>C
ENST00000697150.1:c.1507T>C	ENSP00000513139.1:n.1507T>C
ENST00000697151.1:c.1440T>C	ENSP00000513140.1:n.1440T>C
ENST00000697164.1:c.1520T>C	ENSP00000513153.1:p.Val507Ala
ENST00000697165.1:c.1307T>C	ENSP00000513154.1:p.Val436Ala
ENST00000347310.10:c.1610T>C MANE Select	ENSP00000321345.5:p.Val537Ala
ENST00000637002.1:c.1001T>C	ENSP00000490340.1:p.Val334Ala
ENST00000347310.9:c.1610T>C	ENSP00000321345.5:p.Val537Ala
ENST00000395227.2:c.404T>C	ENSP00000378652.2:p.Val135Ala
ENST00000425614.3:c.845T>C	ENSP00000387640.2:p.Val282Ala
ENST00000473881.2:c.*436T>C	ENSP00000486667.1:n.*436T>C
NM_144701.2:c.1610T>C	NP_653302.2:p.Val537Ala
XM_005270516.2:c.848T>C	XP_005270573.1:p.Val283Ala
XM_011540789.1:c.1700T>C	XP_011539091.1:p.Val567Ala
XM_011540790.1:c.1610T>C	XP_011539092.1:p.Val537Ala
XM_011540791.1:c.1610T>C	XP_011539093.1:p.Val537Ala
XM_011540790.3:c.1610T>C	XP_011539092.1:p.Val537Ala
XM_011540791.3:c.1610T>C	XP_011539093.1:p.Val537Ala
XR_001736993.1:n.1690T>C
NM_144701.3:c.1610T>C MANE Select	NP_653302.2:p.Val537Ala