{{Rsnum
|rsid=33917628
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBB
|position=5226623
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33917628
|variant=0059
}}
{{omim
|id=141900
|rsnum=33917628
|variant=0439
}}{{ClinVar
|rsid=33917628
|Reversed=1
|FwdREF=G
|FwdALT=A,C
|REF=C
|ALT=G,T
|RSPOS=5247853
|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; 2
|CLNHGVS=NC_000011.9:g.5247853C>G; NC_000011.9:g.5247853C>T
|CLNORIGIN=1
|CLNSRCID=
423; 141900.0439; 421; 141900.0059
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000016793.1; RCV000016310.1
|Tags=RV;PM;PMC;S3D;SLO;GNO;OTHERKG;LSD;OM
|CLNDBN=HEMOGLOBIN VILLAVERDE; HEMOGLOBIN CRETEIL
|CLNSRC=HBVAR; OMIM Allelic Variant
|Disease=HEMOGLOBIN VILLAVERDE; HEMOGLOBIN CRETEIL
}}{{PMID Auto
|PMID=6790544
|Title=The structure of hemoglobin Creteil (beta 89 Ser replaced by Asn) is similar to that of abnormal human hemoglobins having sequence changes at Tyr 145 beta.
}}

{{PMID Auto
|PMID=8241293
|Title=Hb Villaverde [beta 89 (F5) Ser-->Thr]: the structural modification of an intrasubunit contact is responsible for a high oxygen affinity.
}}