{{Rsnum
|rsid=36008922
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBB
|position=5226690
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=36008922
|variant=0030
}}
{{omim
|id=141900
|rsnum=36008922
|variant=0447
}}

{{ClinVar
|rsid=36008922
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=5247920
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000102110100
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5247920C>T
|CLNORIGIN=1
|CLNSIG=255
|Tags=RV;PM;PMC;S3D;SLO;GNO;OTHERKG;LSD;OM
|CLNACC=RCV000016276.1; RCV000016801.1
|CLNDBN=HEMOGLOBIN BRISTOL; HEMOGLOBIN ALESHA
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=370; 141900.0030; 141900.0447
|Disease=HEMOGLOBIN BRISTOL; HEMOGLOBIN ALESHA
}}

{{PMID Auto
|PMID=8330974
|Title=Hb Alesha or alpha 2 beta (2)67(E11)Val-->Met: a new unstable hemoglobin variant identified through sequencing of amplified DNA.
}}

{{PMID Auto
|PMID=15646651
|Title=Hb Bristol-Alesha presenting thalassemia-type hyperunstable hemoglobinopathy.
}}

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