Canonical Allele Identifier: CA15080051

Gene: IL23R

Identifiers and link-outs to other resources

• dbSNP Id: rs1004819
• gnomAD: 1:67670213 G / A
• MyVariant Identifiers: chr1:g.67670213G>A (hg19) ; chr1:g.67204530G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67204530G>A , CM000663.2:g.67204530G>A	GRCh38
NC_000001.10:g.67670213G>A , CM000663.1:g.67670213G>A	GRCh37
NC_000001.9:g.67442801G>A	NCBI36
NG_011498.1:g.43045G>A

Transcript Alleles

HGVS	Amino-acid change
NM_144701.2:c.653-2380G>A VV	NP_653302.2:p.=
XM_005270516.2:c.-110-2380G>A	XP_005270573.1:p.=
XM_011540789.1:c.743-2380G>A	XP_011539091.1:p.=
XM_011540790.1:c.653-2380G>A	XP_011539092.1:p.=
XM_011540791.1:c.653-2380G>A	XP_011539093.1:p.=
XM_011540790.3:c.653-2380G>A	XP_011539092.1:p.=
XM_011540791.3:c.653-2380G>A	XP_011539093.1:p.=
XR_001736993.1:n.836-2380G>A
NM_144701.3:c.653-2380G>A VV MANE Preferred	NP_653302.2:p.=
ENST00000347310.9:c.653-2380G>A	ENSP00000321345.5:p.=
ENST00000371007.6:c.-104+27316C>T	ENSP00000360046.1:p.=
ENST00000448166.6:c.-104+27316C>T	ENSP00000415519.2:p.=