Canonical Allele Identifier: CA340728748

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724494C>T (hg19) ; chr1:g.67258811C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67258811C>T , CM000663.2:g.67258811C>T	GRCh38
NC_000001.10:g.67724494C>T , CM000663.1:g.67724494C>T	GRCh37
NC_000001.9:g.67497082C>T	NCBI36
NG_011498.1:g.97326C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1412C>T	ENSP00000513138.1:n.1412C>T
ENST00000697150.1:c.1470C>T	ENSP00000513139.1:n.1470C>T
ENST00000697151.1:c.1403C>T	ENSP00000513140.1:n.1403C>T
ENST00000697164.1:c.1483C>T	ENSP00000513153.1:p.Gln495Ter
ENST00000697165.1:c.1270C>T	ENSP00000513154.1:p.Gln424Ter
ENST00000347310.10:c.1573C>T MANE Select	ENSP00000321345.5:p.Gln525Ter
ENST00000637002.1:c.964C>T	ENSP00000490340.1:p.Gln322Ter
ENST00000347310.9:c.1573C>T	ENSP00000321345.5:p.Gln525Ter
ENST00000395227.2:c.367C>T	ENSP00000378652.2:p.Gln123Ter
ENST00000425614.3:c.808C>T	ENSP00000387640.2:p.Gln270Ter
ENST00000473881.2:c.*399C>T	ENSP00000486667.1:n.*399C>T
NM_144701.2:c.1573C>T	NP_653302.2:p.Gln525Ter
XM_005270516.2:c.811C>T	XP_005270573.1:p.Gln271Ter
XM_011540789.1:c.1663C>T	XP_011539091.1:p.Gln555Ter
XM_011540790.1:c.1573C>T	XP_011539092.1:p.Gln525Ter
XM_011540791.1:c.1573C>T	XP_011539093.1:p.Gln525Ter
XM_011540790.3:c.1573C>T	XP_011539092.1:p.Gln525Ter
XM_011540791.3:c.1573C>T	XP_011539093.1:p.Gln525Ter
XR_001736993.1:n.1653C>T
NM_144701.3:c.1573C>T MANE Select	NP_653302.2:p.Gln525Ter