{{Rsnum
|rsid=34667595
|Chromosome=16
|Orientation=plus
|geno1=(-;-)
|geno2=(-;GAA)
|geno3=(GAA;GAA)
|Gene=HBA2
|position=176947
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA1
}}{{omim
|id=141800
|rsnum=34667595
|variant=0015
}}

{{ClinVar
|ALT=CGAA
|CHROM=16
|CLNACC=RCV000017002.1
|CLNALLE=1
|CLNDBN=HEMOGLOBIN CATONSVILLE
|CLNHGVS=NC_000016.9:g.226946_226947insGAA
|CLNORIGIN=1
|CLNSIG=255
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=141800.0015
|Disease=HEMOGLOBIN CATONSVILLE
|FwdALT=GAA
|GENEINFO=HBA1:3039
|GENE_ID=3039
|GENE_NAME=HBA1
|REF=C
|RSPOS=226946
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050168000000000002110200
|WGT=0
|dbSNPBuildID=126
|rsid=34667595
}}

{{PMID Auto
|PMID=2574721
|Title=Hb Catonsville (glutamic acid inserted between Pro-37(C2)alpha and Thr-38(C3)alpha). Nonallelic gene conversion in the globin system?
}}

{{on chip | 23andMe v3}}