{{Rsnum
|rsid = 28933078
|Gene=HBG1
|Orientation=minus
|ReferenceAllele=A
|MissenseAllele=G
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Chromosome=11
|position=5254429
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBG2
}}{{omim
|desc=HEMOGLOBIN F (SACROMONTE)
|id=142250
|rsnum=28933078
|variant=0038
}}
{{ neighbor
| rsid = 1061234
| distance = 49
}}
{{omim
|id=142250
|rsnum=28933078
|variant=0042
}}{{ClinVar
|ALT=C,G
|CHROM=11
|CLNACC=RCV000016137.1; RCV000016133.1
|CLNALLE=1; 2
|CLNDBN=HEMOGLOBIN F (EMIRATES); HEMOGLOBIN F (SACROMONTE)
|CLNHGVS=NC_000011.9:g.5275659T>C; NC_000011.9:g.5275659T>G
|CLNORIGIN=1
|CLNSIG=255
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=600; 142250.0042; 142250.0038; 142250.0043
|Disease=HEMOGLOBIN F (EMIRATES); HEMOGLOBIN F (SACROMONTE)
|FwdALT=C,G
|FwdREF=A
|GENEINFO=HBG2:3048
|GENE_ID=3048
|GENE_NAME=HBG2
|REF=T
|RSPOS=5275659
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000000000002110100
|WGT=0
|dbSNPBuildID=126
|rsid=28933078
}}{{PMID Auto
|PMID=7558873
|Title=Two fetal hemoglobin variants affecting the same residue: Hb F-Emirates [G gamma 59(E3)Lys-->Glu] and Hb F-Sacromonte [G gamma 59(E3)Lys-->Gln].
}}

{{PMID Auto
|PMID=7687241
|Title=Hb F-Sacromonte or alpha 2G gamma (2)59(E3)Lys-->Gln observed in a Spanish newborn and his mother.
}}