Canonical Allele Identifier: CA23541297

Gene: IL23R C1orf141

Linked Data

• dbSNP Id: rs1001471908
• gnomAD v3: 1-67168043-A-G
• gnomAD v4: 1-67168043-A-G
• MyVariant Identifiers: chr1:g.67633726A>G (hg19) ; chr1:g.67168043A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67168043A>G , CM000663.2:g.67168043A>G	GRCh38
NC_000001.10:g.67633726A>G , CM000663.1:g.67633726A>G	GRCh37
NC_000001.9:g.67406314A>G	NCBI36
NG_011498.1:g.6558A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697222.1:c.-29-49A>G (IL23R)	ENSP00000513189.1:n.-29-49A>G
ENST00000347310.10:c.-29-49A>G (IL23R) MANE Select	ENSP00000321345.5:n.-29-49A>G
ENST00000637002.1:c.-633-49A>G (IL23R)	ENSP00000490340.1:n.-633-49A>G
ENST00000347310.9:c.-29-49A>G (IL23R)	ENSP00000321345.5:n.-29-49A>G
ENST00000371007.6:c.-103-36816T>C (C1orf141)	ENSP00000360046.1:n.-103-36816T>C
ENST00000448166.6:c.-103-36816T>C (C1orf141)	ENSP00000415519.2:n.-103-36816T>C
NM_144701.2:c.-29-49A>G (IL23R)	NP_653302.2:n.-29-49A>G
XM_011540789.1:c.62-49A>G (IL23R)	XP_011539091.1:n.62-49A>G
XM_011540790.1:c.-29-49A>G (IL23R)	XP_011539092.1:n.-29-49A>G
XM_011540791.1:c.-29-49A>G (IL23R)	XP_011539093.1:n.-29-49A>G
XM_011540790.3:c.-29-49A>G (IL23R)	XP_011539092.1:n.-29-49A>G
XM_011540791.3:c.-29-49A>G (IL23R)	XP_011539093.1:n.-29-49A>G
XR_001736993.1:n.155-49A>G (IL23R)
NM_144701.3:c.-29-49A>G (IL23R) MANE Select	NP_653302.2:n.-29-49A>G