Canonical Allele Identifier: CA340729427

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724653G>C (hg19) ; chr1:g.67258970G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258970G>C , CM000663.2:g.67258970G>C	GRCh38
NC_000001.10:g.67724653G>C , CM000663.1:g.67724653G>C	GRCh37
NC_000001.9:g.67497241G>C	NCBI36
NG_011498.1:g.97485G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1571G>C	ENSP00000513138.1:n.1571G>C
ENST00000697150.1:c.1629G>C	ENSP00000513139.1:n.1629G>C
ENST00000697151.1:c.1562G>C	ENSP00000513140.1:n.1562G>C
ENST00000697164.1:c.1642G>C	ENSP00000513153.1:p.Asp548His
ENST00000697165.1:c.1429G>C	ENSP00000513154.1:p.Asp477His
ENST00000347310.10:c.1732G>C MANE Select	ENSP00000321345.5:p.Asp578His
ENST00000637002.1:c.1123G>C	ENSP00000490340.1:p.Asp375His
ENST00000347310.9:c.1732G>C	ENSP00000321345.5:p.Asp578His
ENST00000395227.2:c.526G>C	ENSP00000378652.2:p.Asp176His
ENST00000425614.3:c.967G>C	ENSP00000387640.2:p.Asp323His
ENST00000473881.2:c.*558G>C	ENSP00000486667.1:n.*558G>C
NM_144701.2:c.1732G>C	NP_653302.2:p.Asp578His
XM_005270516.2:c.970G>C	XP_005270573.1:p.Asp324His
XM_011540789.1:c.1822G>C	XP_011539091.1:p.Asp608His
XM_011540790.1:c.1732G>C	XP_011539092.1:p.Asp578His
XM_011540791.1:c.1732G>C	XP_011539093.1:p.Asp578His
XM_011540790.3:c.1732G>C	XP_011539092.1:p.Asp578His
XM_011540791.3:c.1732G>C	XP_011539093.1:p.Asp578His
XR_001736993.1:n.1812G>C
NM_144701.3:c.1732G>C MANE Select	NP_653302.2:p.Asp578His