Variant #0000016127 (NC_000011.9:g.5276169G>A, HBG2(NM_000184.2):c.-211C>T)

Individual ID 00002099
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.5276169G>A
Reference dbSNP
DB-ID HBG2_000008 See all 3 reported entries
Frequency -
Variant remarks -
ClassClinical -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Qianqian Zhang
Database submission license No license selected
Created by Qianqian Zhang
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

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



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000002093 DNA SEQ-NG-I BCL11A, HBA2, HBD, HBE1, HBG1, HBG2, HBS1L, MYB 5 Qi Ming