{{Rsnum
|rsid=63750837
|Chromosome=11
|Orientation=minus
|geno1=(-;-)
|geno2=(-;ACG)
|geno3=(ACG;ACG)
|Gene=HBB
|position=5226597
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=63750837
|variant=0390
}}{{ClinVar
|rsid=63750837
|Reversed=1
|FwdREF=ACG
|FwdALT=ACGT,T
|REF=ACGT
|ALT=A
|RSPOS=5247826
|CHROM=11
|dbSNPBuildID=137
|SSR=0
|SAO=1
|VP=0x050168000000000002110200
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5247827_5247829delCGT
|CLNSIG=255
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000016737.1
|CLNDBN=HEMOGLOBIN GALICIA
|CLNORIGIN=1
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=141900.0390
|Disease=HEMOGLOBIN GALICIA
}}{{PMID Auto
|PMID=2158827
|Title=Hemoglobin Birmingham and hemoglobin Galicia: two unstable beta chain variants characterized by small deletions and insertions.
}}