{{Rsnum
|rsid=267606631
|Chromosome=17
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ACTG1
|position=81511269
|Gene_s=ACTG1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=17
|CLNACC=RCV000019987.26; RCV000059728.1
|CLNALLE=1
|CLNDBN=Deafness, autosomal dominant 20; not provided
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1434:C1858172:604717:90635
|CLNHGVS=NC_000017.10:g.79478295C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|CLNSRCID=102560.0008; VAR_067826
|Disease=Deafness; not provided
|FwdALT=A
|FwdREF=G
|GENEINFO=ACTG1:71
|GENE_ID=71
|GENE_NAME=ACTG1
|REF=C
|RSPOS=79478295
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267606631
}}{{PMID Auto
|PMID=19477959
|Title=In vivo and in vitro effects of two novel gamma-actin (ACTG1) mutations that cause DFNA20/26 hearing impairment.
|OA=1
}}