{{Rsnum
|rsid=35857380
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=HBB
|position=5226785
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=35857380
|variant=0220
}}

{{ClinVar
|rsid=35857380
|Reversed=1
|FwdREF=A
|FwdALT=T
|REF=T
|ALT=A
|RSPOS=5248015
|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
|CLNHGVS=NC_000011.9:g.5248015T>A
|CLNORIGIN=1
|CLNSIG=255
|Tags=RV;PM;PMC;S3D;SLO;GNO;OTHERKG;LSD;OM
|CLNACC=RCV000016550.1
|CLNDBN=HEMOGLOBIN PHILLY
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=141900.0220
|Disease=HEMOGLOBIN PHILLY
}}

{{PMID Auto
|PMID=957431
|Title=Structure and function of haemoglobin Philly (Tyr C1 (35) beta replaced by Phe).
}}

{{PMID Auto
|PMID=5822575
|Title=Hemoglobin Philly (beta 35 tyrosine phenylalanine): studies in the molecular pathology of hemoglobin.
|OA=1
}}

{{PMID Auto
|PMID=9877172
|Title=The artificial alpha1beta1-contact mutant hemoglobin, Hb Phe-35beta, shows only small functional abnormalities.
}}

{{PMID Auto
|PMID=11514675
|Title=Site-directed mutations of human hemoglobin at residue 35beta: a residue at the intersection of the alpha1beta1, alpha1beta2, and alpha1alpha2 interfaces.
|OA=1
}}

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