Canonical Allele Identifier: CA2991933736

Gene: IL23R

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259160T>C , CM000663.2:g.67259160T>C	GRCh38
NC_000001.10:g.67724843T>C , CM000663.1:g.67724843T>C	GRCh37
NC_000001.9:g.67497431T>C	NCBI36
NG_011498.1:g.97675T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_144701.3:c.*32T>C MANE Select	NP_653302.2:n.*32T>C
ENST00000347310.10:c.*32T>C MANE Select	ENSP00000321345.5:n.*32T>C
NM_144701.2:c.*32T>C	NP_653302.2:n.*32T>C
ENST00000347310.9:c.*32T>C	ENSP00000321345.5:n.*32T>C
ENST00000395227.2:c.*32T>C	ENSP00000378652.2:n.*32T>C
ENST00000425614.3:c.*32T>C	ENSP00000387640.2:n.*32T>C
ENST00000473881.2:c.*748T>C	ENSP00000486667.1:n.*748T>C
ENST00000637002.1:c.*32T>C	ENSP00000490340.1:n.*32T>C
XM_005270516.2:c.*32T>C	XP_005270573.1:n.*32T>C
XM_011540789.1:c.*32T>C	XP_011539091.1:n.*32T>C
XM_011540790.1:c.*32T>C	XP_011539092.1:n.*32T>C
XM_011540790.3:c.*32T>C	XP_011539092.1:n.*32T>C
XM_011540791.1:c.*32T>C	XP_011539093.1:n.*32T>C
XM_011540791.3:c.*32T>C	XP_011539093.1:n.*32T>C