Variant #0000000154 (NC_000011.9:g.5275533C>G, HBG2(NM_000184.2):c.304G>C)

Chromosome 11
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Substitution
DNA change (genomic) (Relative to hg19 / GRCh37) g.5275533C>G
Reference dbSNP;
DB-ID HBG2_000013 See all 5 reported entries
Frequency -
Variant remarks Hb F-Zhejang
ClassClinical Uncertain significance
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HBG2 NM_000184.2 ./. 02 c.304G>C r.(?) p.(Glu102Gln)