{{Rsnum
|rsid=34068598
|Chromosome=16
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=HBA2
|position=176999
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA1
}}{{omim
|id=141800
|rsnum=34068598
|variant=0204
}}{{ClinVar
|rsid=34068598
|Reversed=0
|FwdREF=G
|FwdALT=C
|REF=G
|ALT=C
|RSPOS=226998
|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
|CLNHGVS=NC_000016.9:g.226998G>C
|CLNORIGIN=1
|CLNSIG=255
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000017223.1
|CLNDBN=HEMOGLOBIN ROUBAIX
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=796; 141800.0204
|Disease=HEMOGLOBIN ROUBAIX
}}{{PMID Auto
|PMID=10569725
|Title=Hb Roubaix [alpha55(E4)Val-->Leu]: a new neutral hemoglobin variant involving the alpha1 gene.
}}

{{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)].
}}