Canonical Allele Identifier: CA738095296

Gene: IL23R

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259366T>C , CM000663.2:g.67259366T>C	GRCh38
NC_000001.10:g.67725049T>C , CM000663.1:g.67725049T>C	GRCh37
NC_000001.9:g.67497637T>C	NCBI36
NG_011498.1:g.97881T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347310.10:c.*238T>C MANE Select	ENSP00000321345.5:n.*238T>C
ENST00000347310.9:c.*238T>C	ENSP00000321345.5:n.*238T>C
ENST00000395227.2:c.*238T>C	ENSP00000378652.2:n.*238T>C
ENST00000473881.2:c.*954T>C	ENSP00000486667.1:n.*954T>C
NM_144701.2:c.*238T>C	NP_653302.2:n.*238T>C
XM_005270516.2:c.*238T>C	XP_005270573.1:n.*238T>C
XM_011540789.1:c.*238T>C	XP_011539091.1:n.*238T>C
XM_011540790.1:c.*238T>C	XP_011539092.1:n.*238T>C
XM_011540791.1:c.*238T>C	XP_011539093.1:n.*238T>C
XM_011540790.3:c.*238T>C	XP_011539092.1:n.*238T>C
XM_011540791.3:c.*238T>C	XP_011539093.1:n.*238T>C
NM_144701.3:c.*238T>C MANE Select	NP_653302.2:n.*238T>C