{{Rsnum
|rsid=33965000
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HBB
|position=5226590
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33965000
|variant=0028
}}
{{omim
|id=141900
|rsnum=33965000
|variant=0195
}}{{ClinVar
|rsid=33965000
|Reversed=1
|FwdREF=C
|FwdALT=G,T
|REF=G
|ALT=A,C
|RSPOS=5247820
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000011.9:g.5247820G>A; NC_000011.9:g.5247820G>C
|CLNORIGIN=1
|CLNSRCID=
459; 141900.0028; 460; 141900.0195
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000016271.1; RCV000016515.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDBN=HEMOGLOBIN BRIGHAM; HEMOGLOBIN NEW MEXICO
|CLNSRC=HBVAR; OMIM Allelic Variant
|Disease=HEMOGLOBIN BRIGHAM; HEMOGLOBIN NEW MEXICO
}}{{PMID Auto
|PMID=4719677
|Title=Hemoglobin brigham (alpha2Abeta2100 Pro--Leu). Hemoglobin variant associated with familial erythrocytosis.
|OA=1
}}

{{PMID Auto
|PMID=3840697
|Title=Hemoglobin New Mexico: beta 100 (G2) Pro----Arg. A variant hemoglobin associated with erythrocytosis.
}}