{{Rsnum
|rsid=34708054
|Chromosome=16
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=HBA2
|position=176777
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA1
}}{{omim
|id=141800
|rsnum=34708054
|variant=0104
}}
{{omim
|id=141850
|rsnum=34708054
|variant=0042
}}{{ClinVar
|rsid=34708054
|Reversed=0
|FwdREF=C
|FwdALT=G,T
|REF=C
|ALT=G,T
|RSPOS=226776
|CHROM=16
|dbSNPBuildID=126
|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.226776C>T
|CLNORIGIN=1
|CLNSRCID=
26; 141800.0104
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000017118.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDBN=HEMOGLOBIN NECKER ENFANTS-MALADES
|CLNSRC=HBVAR; OMIM Allelic Variant
|Disease=HEMOGLOBIN NECKER ENFANTS-MALADES
}}{{PMID Auto
|PMID=7390863
|Title=A silent hemoglobin variant: hemoglobin necker enfants-malades alpha 20 (B1) His leads to Tyr.
}}