{{Rsnum
|rsid=397515326
|Chromosome=7
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=HNRNPA2B1
|position=26193346
|Gene_s=HNRNPA2B1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=7
|CLNACC=RCV000055652.5
|CLNALLE=1
|CLNDBN=Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=CN180154:615422
|CLNHGVS=NC_000007.13:g.26232966T>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=600124.0001
|Disease=Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2
|FwdALT=T
|FwdREF=A
|GENEINFO=HNRNPA2B1:3181
|GENE_ID=3181
|GENE_NAME=HNRNPA2B1
|REF=T
|RSPOS=26232966
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397515326
}}