{{Rsnum
|rsid=63750968
|Chromosome=11
|Orientation=minus
|geno1=(-;-)
|geno2=(-;GGCCTG)
|geno3=(GGCCTG;GGCCTG)
|Gene=HBB
|position=5226664
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=63750968
|variant=0267
}}{{ClinVar
|rsid=63750968
|Reversed=1
|FwdREF=GCCTGG
|FwdALT=GGCCTGG,G
|REF=CCAGGCC
|ALT=C
|RSPOS=5247893
|CHROM=11
|dbSNPBuildID=137
|SSR=0
|SAO=1
|VP=0x050168000000000002110200
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5247894_5247899delCAGGCC
|CLNSIG=255
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000016610.1
|CLNDBN=HEMOGLOBIN ST. ANTOINE
|CLNORIGIN=1
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=727; 141900.0267
|Disease=HEMOGLOBIN ST. ANTOINE
}}{{PMID Auto
|PMID=4699574
|Title=Two new hemoglobin variants with deletion. Hemoglobin tours: Thr 8 7 (F 3 ) deleted and hemoglobin St Antoine: Gly-Leu 74-75 (E 18-19 deleted. Consequences for oxygen affinity and protein stability.
}}