Canonical Allele Identifier: CA15702351
Gene: IL18 HGNC NCBI
gnomAD v2:
11:112026703 A / G
gnomAD v3:
11:112155980 A / G
gnomAD v4:
chr11-112155980-A-G
Joint Max Group AF 0.88052676 (SAS)
Genomes Max Group AF 0.88052676 (SAS)
ClinVar RCV:
RCV001003439
ClinVar Variation:
812623
dbSNP:
360722
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112155980A>G , CM000673.2:g.112155980A>G GRCh38
NC_000011.9:g.112026703A>G , CM000673.1:g.112026703A>G GRCh37
NC_000011.8:g.111531913A>G NCBI36
NG_028143.1:g.13138T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000280357.12:c.-8-919T>C MANE Select ENSP00000280357.7:n.-8-919T>C
ENST00000280357.11:c.-8-919T>C ENSP00000280357.7:n.-8-919T>C
ENST00000524595.5:c.-8-919T>C ENSP00000434561.1:n.-8-919T>C
ENST00000525987.5:n.320-14439A>G
ENST00000528832.1:c.-29-898T>C ENSP00000434161.1:n.-29-898T>C
ENST00000531744.5:c.315-14439A>G ENSP00000456957.1:n.315-14439A>G
ENST00000532699.1:c.315-14439A>G ENSP00000456434.1:n.315-14439A>G
ENST00000533858.5:n.192-919T>C
ENST00000534225.1:n.189-919T>C
NM_001243211.1:c.-8-919T>C NP_001230140.1:n.-8-919T>C
NM_001562.3:c.-8-919T>C NP_001553.1:n.-8-919T>C
XM_011542805.1:c.-29-898T>C XP_011541107.1:n.-29-898T>C
XM_011542806.1:c.-29-898T>C XP_011541108.1:n.-29-898T>C
XM_011542806.2:c.-29-898T>C XP_011541108.1:n.-29-898T>C
NM_001562.4:c.-8-919T>C MANE Select NP_001553.1:n.-8-919T>C
NM_001243211.2:c.-8-919T>C NP_001230140.1:n.-8-919T>C
NM_001386420.1:c.-29-898T>C NP_001373349.1:n.-29-898T>C
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