Canonical Allele Identifier: CA2646126032

Gene: IL23R

Linked Data

• gnomAD v4: 1-67259319-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259319T>C , CM000663.2:g.67259319T>C	GRCh38
NC_000001.10:g.67725002T>C , CM000663.1:g.67725002T>C	GRCh37
NC_000001.9:g.67497590T>C	NCBI36
NG_011498.1:g.97834T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000347310.10:c.*191T>C MANE Select	ENSP00000321345.5:n.*191T>C
ENST00000347310.9:c.*191T>C	ENSP00000321345.5:n.*191T>C
ENST00000395227.2:c.*191T>C	ENSP00000378652.2:n.*191T>C
ENST00000473881.2:c.*907T>C	ENSP00000486667.1:n.*907T>C
NM_144701.2:c.*191T>C	NP_653302.2:n.*191T>C
XM_005270516.2:c.*191T>C	XP_005270573.1:n.*191T>C
XM_011540789.1:c.*191T>C	XP_011539091.1:n.*191T>C
XM_011540790.1:c.*191T>C	XP_011539092.1:n.*191T>C
XM_011540791.1:c.*191T>C	XP_011539093.1:n.*191T>C
XM_011540790.3:c.*191T>C	XP_011539092.1:n.*191T>C
XM_011540791.3:c.*191T>C	XP_011539093.1:n.*191T>C
NM_144701.3:c.*191T>C MANE Select	NP_653302.2:n.*191T>C