{{Rsnum
|rsid = 28928881
|Gene = HBA1
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=T
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Chromosome=16
|position=177352
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA1
}}{{omim
|desc=HEMOGLOBIN MALHACEN
|id=141800
|rsnum=28928881
|variant=0190
}}
{{ neighbor
| rsid = 28928884
| distance = 60
}}

{{ClinVar
|rsid=28928881
|Reversed=0
|FwdREF=G
|FwdALT=C,T
|REF=G
|ALT=C,T
|RSPOS=227351
|CHROM=16
|dbSNPBuildID=133
|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.227351G>T
|CLNORIGIN=1
|CLNSIG=255
|CLNCUI=
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000017210.1
|CLNDBN=HEMOGLOBIN MALHACEN
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=186; 141800.0190
|Disease=HEMOGLOBIN MALHACEN
}}

{{PMID Auto
|PMID=7615398
|Title=Hb Anamosa or alpha 2(111)(G18)Ala-->Val beta 2 (alpha 2 mutation) and Hb Mulhacen or alpha 2(123)(H6)Ala-->Ser beta 2 (alpha 1 mutation) are two silent, stable variants detected by sequencing of amplified DNA.
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}