{{Rsnum
|rsid=33983276
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=HBB
|position=5225668
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33983276
|variant=0148
}}
{{omim
|id=141900
|rsnum=33983276
|variant=0289
}}
{{omim
|id=141900
|rsnum=33983276
|variant=0481
}}{{ClinVar
|rsid=33983276
|Reversed=1
|FwdREF=C
|FwdALT=A,G,T
|REF=G
|ALT=A,C,T
|RSPOS=5246898
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000002110104
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=1; 2; 3
|CLNHGVS=NC_000011.9:g.5246898G>A; NC_000011.9:g.5246898G>C; NC_000011.9:g.5246898G>T
|CLNORIGIN=1
|CLNSRCID=
518; 141900.0481; 515; 141900.0148; 516; 141900.0289
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000016836.1; RCV000016438.1; RCV000016632.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM;NOV
|CLNDBN=HEMOGLOBIN TENDE; HEMOGLOBIN KHARTOUM; HEMOGLOBIN TY GARD
|CLNSRC=HBVAR; OMIM Allelic Variant
|Disease=HEMOGLOBIN TENDE; HEMOGLOBIN KHARTOUM; HEMOGLOBIN TY GARD
}}{{PMID Auto
|PMID=639985
|Title=Hemoglobin Ty GARD (alphaA2beta2 124 (H2) Pro replaced by Gln). A stable high O2 affinity variant at the alpha1beta1 contact.
}}

{{PMID Auto
|PMID=9859935
|Title=Hb Tende [beta124(H2)Pro-->Leu]: a new variant with a moderate increase in oxygen affinity.
}}