Canonical Allele Identifier: CA340729875

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724761C>T (hg19) ; chr1:g.67259078C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259078C>T , CM000663.2:g.67259078C>T	GRCh38
NC_000001.10:g.67724761C>T , CM000663.1:g.67724761C>T	GRCh37
NC_000001.9:g.67497349C>T	NCBI36
NG_011498.1:g.97593C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1679C>T	ENSP00000513138.1:n.1679C>T
ENST00000697150.1:c.1737C>T	ENSP00000513139.1:n.1737C>T
ENST00000697151.1:c.1670C>T	ENSP00000513140.1:n.1670C>T
ENST00000697164.1:c.1750C>T	ENSP00000513153.1:p.Gln584Ter
ENST00000697165.1:c.1537C>T	ENSP00000513154.1:p.Gln513Ter
ENST00000347310.10:c.1840C>T MANE Select	ENSP00000321345.5:p.Gln614Ter
ENST00000637002.1:c.1231C>T	ENSP00000490340.1:p.Gln411Ter
ENST00000347310.9:c.1840C>T	ENSP00000321345.5:p.Gln614Ter
ENST00000395227.2:c.634C>T	ENSP00000378652.2:p.Gln212Ter
ENST00000425614.3:c.1075C>T	ENSP00000387640.2:p.Gln359Ter
ENST00000473881.2:c.*666C>T	ENSP00000486667.1:n.*666C>T
NM_144701.2:c.1840C>T	NP_653302.2:p.Gln614Ter
XM_005270516.2:c.1078C>T	XP_005270573.1:p.Gln360Ter
XM_011540789.1:c.1930C>T	XP_011539091.1:p.Gln644Ter
XM_011540790.1:c.1840C>T	XP_011539092.1:p.Gln614Ter
XM_011540791.1:c.1840C>T	XP_011539093.1:p.Gln614Ter
XM_011540790.3:c.1840C>T	XP_011539092.1:p.Gln614Ter
XM_011540791.3:c.1840C>T	XP_011539093.1:p.Gln614Ter
XR_001736993.1:n.1920C>T
NM_144701.3:c.1840C>T MANE Select	NP_653302.2:p.Gln614Ter