{{Rsnum
|rsid=266257354
|Chromosome=15
|Orientation=minus
|geno1=(-;-)
|geno2=(-;G)
|geno3=(G;G)
|Gene=EPB42
|position=43216289
|Gene_s=EPB42
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=15
|CLNACC=RCV000033190.24
|CLNALLE=1
|CLNDBN=Spherocytosis type 5
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2675192:612690:822
|CLNHGVS=NC_000015.9:g.43508487delC
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=177070.0002
|Disease=Spherocytosis type 5
|FwdREF=G
|GENEINFO=EPB42:2038
|GENE_ID=2038
|GENE_NAME=EPB42
|REF=AC
|RSPOS=43508486
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;S3D;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050268000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=266257354
}}{{PMID Auto
|PMID=7803799
|Title=A deletional frameshift mutation in protein 4.2 gene (allele 4.2 Lisboa) associated with hereditary hemolytic anemia.
}}