Variant #0001820655 (NC_000019.9:g.58864610del, NC_000019.9(NM_130786.3):c.71-47del (A1BG))

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.58864610del
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID A1BG_000095
Frequency 65/12516
Freq. EA 12/8252
Freq. AA 53/4264
Average frequency (gnomAD v.2.1.1) -
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-05-03 16:45:39 +02:00 (CEST)
Date last edited 2018-08-22 05:21:47 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
A1BG NM_130786.3 ?/? c.71-47del r.(=) p.(=)
A1BG-AS1 NR_015380.1 ?/? n.1076-135del r.(=) p.(=)