Variant #0000000117 (NC_000011.9:g.5276169G>A, HBG2(NM_000184.2):c.-211C>T)

Chromosome 11
Allele Both (homozygous)
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Type Substitution
DNA change (genomic) (Relative to hg19 / GRCh37) g.5276169G>A
Reference GenBank;dbSNP
DB-ID HBG2_000008 See all 3 reported entries
Frequency -
Variant remarks -
ClassClinical uncertain significance
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HBG2 NM_000184.2 ./. - c.-211C>T r.(=) p.(=)