{{Rsnum
|rsid=34878913
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HBG1
|position=5254482
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBG2
}}{{omim
|id=142250
|rsnum=34878913
|variant=0041
}}{{ClinVar
|ALT=G
|CHROM=11
|CLNACC=RCV000016136.24
|CLNALLE=1
|CLNDBN=Cyanosis, transient neonatal
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C3151421:613977:280615
|CLNHGVS=NC_000011.9:g.5275712A>G
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=596; 142250.0041
|Disease=Cyanosis
|FwdALT=C
|FwdREF=T
|GENEINFO=HBG2:3048
|GENE_ID=3048
|GENE_NAME=HBG2
|REF=A
|RSPOS=5275712
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000000000002110100
|WGT=0
|dbSNPBuildID=126
|rsid=34878913
}}

{{PMID Auto
|PMID=7741137
|Title=Hemoglobin F-Cincinnati, alpha 2G gamma 2 41(C7) Phe-->Ser in a newborn with cyanosis.
}}

{{on chip | 23andMe v4}}