{{Rsnum
|rsid=34890875
|Chromosome=16
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=HBA2
|position=176957
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA1
}}{{omim
|id=141800
|rsnum=34890875
|variant=0099
}}{{ClinVar
|ALT=T
|CHROM=16
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.226956A>T
|CLNORIGIN=1
|CLNSIG=255
|FwdALT=T
|FwdREF=A
|GENEINFO=HBA1:3039
|GENE_ID=3039
|GENE_NAME=HBA1
|REF=A
|RSPOS=226956
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000000000002110100
|WGT=0
|dbSNPBuildID=126
|rsid=34890875
|CLNACC=RCV000017115.1
|CLNDBN=HEMOGLOBIN MIYANO
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=141800.0099
|Disease=HEMOGLOBIN MIYANO
}}

{{PMID Auto
|PMID=2634665
|Title=Hb Miyano or alpha 41(C6)Thr----Ser: a new high oxygen affinity alpha chain variant found in an erythremic blood donor.
}}

{{on chip | 23andMe v4}}