{{Rsnum
|rsid=34440919
|Chromosome=16
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=HBA2
|position=177070
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA1
}}{{omim
|id=141800
|rsnum=34440919
|variant=0139
}}{{ClinVar
|ALT=G
|CHROM=16
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.227069C>G
|CLNORIGIN=1
|CLNSIG=255
|FwdALT=G
|FwdREF=C
|GENEINFO=HBA1:3039
|GENE_ID=3039
|GENE_NAME=HBA1
|REF=C
|RSPOS=227069
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000000000002110100
|WGT=0
|dbSNPBuildID=126
|rsid=34440919
|CLNACC=RCV000017160.1
|CLNDBN=HEMOGLOBIN STANLEYVILLE-II
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=141800.0139
|Disease=HEMOGLOBIN STANLEYVILLE-II
}}

{{PMID Auto
|PMID=807076
|Title=Haemoglobin Stanleyville II (alpha75 [EF 7] Asn yeilds Lys) found in France.
}}

{{PMID Auto
|PMID=5696551
|Title=Haemoglobin Stanleyville II (alpha asparagine replaced by lysine).
|OA=1
}}

{{PMID Auto
|PMID=6681956
|Title=Sickle cell hemoglobin fiber formation strongly inhibited by the Stanleyville II mutation (alpha 78 Asn leads to Lys).
}}

{{on chip | 23andMe v4}}