Variant #0000000326 (NC_000011.9:g.5248250A>G, HBB(NM_000518.4):c.2T>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.5248250A>G
Reference Zhang et al;(OMIM 0345);dbSNP
DB-ID HBB_000033
Frequency -
Variant remarks Initiation codon ATG->ACG
ClassClinical Pathogenic
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     
HBB NM_000518.4 ./. 01 c.2T>C r.? p.?