{{Rsnum
|rsid=386134182
|Chromosome=2
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=ALS2
|position=201744431
|Gene_s=ALS2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=2
|CLNACC=RCV000034887.1
|CLNALLE=1
|CLNDBN=Infantile-onset ascending hereditary spastic paralysis
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1243:C1846588:607225:293168
|CLNHGVS=NC_000002.11:g.202609154T>A
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK1243
|Disease=Infantile-onset ascending hereditary spastic paralysis
|FwdALT=T
|FwdREF=A
|REF=T
|RSPOS=202609154
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050168000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=386134182
|GENEINFO=ALS2:57679
|GENE_ID=57679
|GENE_NAME=ALS2
}}{{PMID Auto
|PMID=18810511
|Title=Maternal uniparental heterodisomy with partial isodisomy of a chromosome 2 carrying a splice acceptor site mutation (IVS9-2A>T) in ALS2 causes infantile-onset ascending spastic paralysis (IAHSP).
}}