Variant #0000000155 (NC_000011.9:g.5274949del, HBG2(NM_000184.2):c.316-314del)

Chromosome 11
Allele Parent #1
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Type Deletion
DNA change (genomic) (Relative to hg19 / GRCh37) g.5274949del
Reference Cai et al
DB-ID HBG2_000015
Frequency -
Variant remarks Uncertain significant; Fushion
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 ./. 03 c.316-314del r.(=) p.(=)