{{Rsnum
|rsid=34814612
|Chromosome=16
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=HBA2
|position=177118
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA1
}}{{omim
|id=141800
|rsnum=34814612
|variant=0189
}}{{ClinVar
|ALT=G
|CHROM=16
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.227117C>G
|CLNORIGIN=1
|CLNSIG=255
|FwdALT=G
|FwdREF=C
|GENEINFO=HBA1:3039
|GENE_ID=3039
|GENE_NAME=HBA1
|REF=C
|RSPOS=227117
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000000000002110100
|WGT=0
|dbSNPBuildID=126
|rsid=34814612
|CLNACC=RCV000017209.1
|CLNDBN=HEMOGLOBIN ROANNE
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=141800.0189
|Disease=HEMOGLOBIN ROANNE
}}{{PMID Auto
|PMID=7811728
|Title=Hemoglobin Roanne [alpha 94(G1) Asp-->Glu]: a variant of the alpha 1 beta 2 interface with an unexpected high oxygen affinity.
}}