Variant #0000000371 (NC_000011.9:g.5248184T>G, HBB(NM_000518.4):c.68A>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.5248184T>G
Reference (OMIM 0081);dbSNP;Li J et al.;el-Hashemite N et al.;Dincol G et al.;Blackwell RQ et al.;
DB-ID HBB_000049
Frequency -
Variant remarks Hb G-Coushatta
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     
HBB NM_000518.4 ./. 01 c.68A>C r.(?) p.(Glu23Ala)