{{Rsnum
|rsid=33935328
|Chromosome=16
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=HBA1
|position=177407
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA1
}}{{omim
|id=141800
|rsnum=33935328
|variant=0087
}}
{{omim
|id=141800
|rsnum=33935328
|variant=0135
}}
{{omim
|id=141800
|rsnum=33935328
|variant=0144
}}

{{ClinVar
|rsid=33935328
|Reversed=0
|FwdREF=G
|FwdALT=A,C,T
|REF=G
|ALT=A,C,T
|RSPOS=227406
|CHROM=16
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000402110100
|GENEINFO=HBA1:3039
|GENE_NAME=HBA1
|GENE_ID=3039
|WGT=0
|VC=SNV
|CLNALLE=1; 2; 3
|CLNHGVS=NC_000016.9:g.227406G>A; NC_000016.9:g.227406G>C; NC_000016.9:g.227406G>T
|CLNORIGIN=1
|CLNSRCID=
212; 141800.0144; 211; 141800.0135; 214; 141800.0087
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000017164.1; RCV000017157.1; RCV000017093.1
|Tags=PM;PMC;S3D;SLO;HD;OTHERKG;LSD;OM
|CLNDBN=HEMOGLOBIN SURESNES; HEMOGLOBIN SINGAPORE; HEMOGLOBIN LEGNANO
|CLNSRC=HBVAR; OMIM Allelic Variant
|Disease=HEMOGLOBIN SURESNES; HEMOGLOBIN SINGAPORE; HEMOGLOBIN LEGNANO
}}

{{PMID Auto
|PMID=5782115
|Title=Two new haemoglobin variants involving proline substitutions.
}}

{{PMID Auto
|PMID=11123
|Title=Structural and functional studies of haemoglobin Suresnes or alpha2 141 (HC3) Arg replaced by His beta2, a new high oxygen affinity mutant.
}}

{{PMID Auto
|PMID=640857
|Title=Hb Suresnes or alpha2 141(HC3) ArgyieldHis beta2 in a black family.
}}

{{PMID Auto
|PMID=7410435
|Title=Structural and functional studies of hemoglobin Suresnes (arg 141 alpha 2 replaced by His beta 2). Consequences of disrupting an oxygen-linked anion-binding site.
}}

{{PMID Auto
|PMID=701083
|Title=Hemoglobin Legnano (alpha2 141 (HC3) Arg replaced by Leu beta2): a new abnormal human hemoglobin with high oxygen affinity.
}}

{{on chip | Illumina Human 1M}}