HGVS | Genome Assembly |
---|---|
NC_000003.12:g.169764852C>A , CM000665.2:g.169764852C>A | GRCh38 |
NC_000003.11:g.169482640C>A , CM000665.1:g.169482640C>A | GRCh37 |
NC_000003.10:g.170965334C>A | NCBI36 |
NG_016363.1:g.5209G>T , LRG_347:g.5209G>T |
HGVS | Amino-acid Change | |
---|---|---|
NR_001566.1:n.209G>T , LRG_347t1:n.209G>T |