{{Rsnum
|rsid=41323248
|Chromosome=16
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HBA2
|position=173229
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA2
}}{{omim
|id=141850
|rsnum=41323248
|variant=0045
}}

{{ClinVar
|rsid=41323248
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=223228
|CHROM=16
|dbSNPBuildID=127
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=HBA2:3040
|GENE_NAME=HBA2
|GENE_ID=3040
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.223228T>C
|CLNORIGIN=1
|CLNSIG=255
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000016955.1
|CLNDBN=HEMOGLOBIN DARTMOUTH
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=141850.0045
|Disease=HEMOGLOBIN DARTMOUTH
}}

{{PMID Auto
|PMID=11791870
|Title=Hb Dartmouth [alpha66(E15)Leu-->Pro (alpha2) (CTG-->CCG)]: a novel alpha2-globin gene mutation associated with severe neonatal anemia when inherited in trans with Southeast Asian alpha-thalassemia-1.
}}

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