{{Rsnum
|rsid=41417548
|Chromosome=16
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBA2
|position=173485
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA2
}}{{omim
|id=141850
|rsnum=41417548
|variant=0031
}}

{{ClinVar
|rsid=41417548
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=223484
|CHROM=16
|dbSNPBuildID=127
|SSR=0
|SAO=1
|VP=0x050368000000000102110100
|GENEINFO=HBA2:3040
|GENE_NAME=HBA2
|GENE_ID=3040
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.223484G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=141850.0031
|CLNSIG=255
|CLNCUI=CN077787
|CLNDBN=HEMOGLOBIN SALLANCHES; Hemoglobin H disease, nondeletional
|Disease=HEMOGLOBIN SALLANCHES; Hemoglobin H disease
|CLNACC=RCV000016942.1; RCV000022606.1
|Tags=PM;PMC;S3D;SLO;GNO;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=CN077787
}}

{{PMID Auto
|PMID=8555062
|Title=A new alpha chain variant Hb Sallanches [alpha 2 104(G11) Cys-->Tyr] associated with HbH disease in one homozygous patient.
}}

{{PMID Auto
|PMID=10722113
|Title=Hb Sallanches [alpha104(G11)Cys-->Tyr]: a rare alpha2-globin chain variant found in the homozygous state in three members of a Pakistani family.
}}

{{PMID Auto
|PMID=11186268
|Title=Homozygous Hb Sallanches [alpha104(G11)Cys-->Tyr] in a Pakistani child with Hb H disease.
}}

{{PMID Auto
|PMID=16840231
|Title=Hb Sallanches [alpha104(G11)Cys-->Tyr, TGC-->TAC (alpha2)]: an unstable hemoglobin variant found in an Indian child.
}}

{{PMID Auto
|PMID=20113287
|Title=Hb H disease due to homozygosity for a rare alpha2-globin variant, Hb Sallanches.
}}

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