{{Rsnum
|rsid=266257355
|Chromosome=15
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=EPB42
|position=43209273
|Gene_s=EPB42
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=15
|CLNACC=RCV000014141.24
|CLNALLE=1
|CLNDBN=Spherocytosis type 5
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2675192:612690:822
|CLNHGVS=NC_000015.9:g.43501471C>T
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=177070.0004
|Disease=Spherocytosis type 5
|FwdALT=A
|FwdREF=G
|GENEINFO=EPB42:2038
|GENE_ID=2038
|GENE_NAME=EPB42
|REF=C
|RSPOS=43501471
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=266257355
}}{{PMID Auto
|PMID=8528207
|Title=A novel mutation causing an aberrant splicing in the protein 4.2 gene associated with hereditary spherocytosis (protein 4.2Notame).
}}