{{Rsnum
|rsid = 1061009
|Gene=HBA1
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=G
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Chromosome=16
|position=177103
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA2
}}{{omim
|desc=HEMOGLOBIN BUFFALO
|id=141800
|rsnum=1061009
|variant=0212
}}
{{ neighbor
| rsid = 28928887
| distance = 87
}}
{{ neighbor
| rsid = 28928889
| distance = 204
}}{{ClinVar
|rsid=1061009
|Reversed=0
|FwdREF=C
|FwdALT=A,G
|REF=C
|ALT=A,G
|RSPOS=227102
|CHROM=16
|dbSNPBuildID=86
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=HBA1:3039
|GENE_NAME=HBA1
|GENE_ID=3039
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000016.9:g.227102C>G
|CLNORIGIN=1
|CLNSIG=255
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000017231.1
|CLNDBN=HEMOGLOBIN BUFFALO
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=141800.0212
|Disease=HEMOGLOBIN BUFFALO
}}{{PMID Auto
|PMID=11482884
|Title=Rapid identification of hemoglobin variants by electrospray ionization mass spectrometry.
}}

{{PMID Auto
|PMID=12403494
|Title=Three new variants of the alpha1-globin gene without clinical or hematologic effects: Hb Hagerstown [alpha44(CE2)Pro-->Ala (alpha1)]; Hb Buffalo [alpha89(FG1)His-->Gln (alpha1)], a hemoglobin variant from Somalia and Yemen; Hb Wichita [alpha95(G2)Pro-->Gln (alpha1)]; and a second, unrelated, case of Hb Roubaix [alpha55(E4)Val-->Leu (alpha1)].
}}

{{PMID Auto
|PMID=15481890
|Title=Hb Buffalo [alpha89(FG1)His-->Gln (alpha1)], observed solely and in the presence of an Hb S [beta6(A3)Glu-->Val] heterozygosity.
}}