{{Rsnum
|rsid=35521813
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=HBG1
|position=5254704
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBG2
}}{{omim
|id=142250
|rsnum=35521813
|variant=0001
}}{{ClinVar
|ALT=C,G
|CHROM=11
|CLNALLE=2
|CLNHGVS=NC_000011.9:g.5275934T>G
|CLNORIGIN=1
|CLNSIG=255
|FwdALT=C,G
|FwdREF=A
|GENEINFO=HBG2:3048
|GENE_ID=3048
|GENE_NAME=HBG2
|REF=T
|RSPOS=5275934
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000000000002110100
|WGT=0
|dbSNPBuildID=126
|rsid=35521813
|CLNACC=RCV000016097.1
|CLNDBN=HEMOGLOBIN F (ALBAICIN)
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=142250.0001
|Disease=HEMOGLOBIN F (ALBAICIN)
}}{{PMID Auto
|PMID=2435680
|Title=Hb F-Albaicin or G gamma 8(A5)Lys----Glu or Gln.
}}