{{Rsnum
|rsid=63749797
|Chromosome=11
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=HBG1
|position=5248394
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBG1
}}{{omim
|id=142200
|rsnum=63749797
|variant=0037
}}

{{ClinVar
|rsid=63749797
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=5269624
|CHROM=11
|dbSNPBuildID=137
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=HBG1:3047
|GENE_NAME=HBG1
|GENE_ID=3047
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5269624C>A
|CLNORIGIN=1
|CLNSIG=255
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000016185.1
|CLNDBN=HEMOGLOBIN F (PORTO TORRES)
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=142200.0037
|Disease=HEMOGLOBIN F (PORTO TORRES)
}}

{{PMID Auto
|PMID=15666429
|Title=Hb F-Porto Torres [Agamma75(E19)Ile-->Thr, 136(H14)Ala-->Ser]: a novel variant of the Agamma chain having two substitutions, one being that of Hb F-Sardinia.
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}