{{Rsnum
|rsid=33978134
|Chromosome=16
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=HBA2
|position=176967
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA1
}}{{omim
|id=141800
|rsnum=33978134
|variant=0082
}}
{{omim
|id=141800
|rsnum=33978134
|variant=0098
}}{{ClinVar
|rsid=33978134
|Reversed=0
|FwdREF=C
|FwdALT=G,T
|REF=C
|ALT=G,T
|RSPOS=226966
|CHROM=16
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=HBA1:3039
|GENE_NAME=HBA1
|GENE_ID=3039
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000016.9:g.226966C>G; NC_000016.9:g.226966C>T
|CLNORIGIN=1
|CLNSRCID=
58; 141800.0082; 57; 141800.0098
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000017080.1; RCV000017114.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDBN=HEMOGLOBIN KAWACHI; HEMOGLOBIN MILLEDGEVILLE
|CLNSRC=HBVAR; OMIM Allelic Variant
|Disease=HEMOGLOBIN KAWACHI; HEMOGLOBIN MILLEDGEVILLE
}}{{PMID Auto
|PMID=7213661
|Title=Hemoglobin Milledgeville (alpha 44 (CD2) Pro leads to Leu): a new variant with increased oxygen affinity.
}}

{{PMID Auto
|PMID=12403493
|Title=Thrombotic events in compound heterozygotes for a high affinity hemoglobin variant: Hb Milledgeville [alpha44(CE2)Pro-->Leu (alpha2)] and factor V Leiden.
}}

{{PMID Auto
|PMID=7068434
|Title=Hemoglobin Kawachi [alpha 44 (CE2) Pro leads to Arg]: a new hemoglobin variant of high oxygen affinity with amino acid substitution at alpha 1 beta 2 contact.
}}