HGVS | Genome Assembly |
---|---|
NC_000003.12:g.169764893T>A , CM000665.2:g.169764893T>A | GRCh38 |
NC_000003.11:g.169482681T>A , CM000665.1:g.169482681T>A | GRCh37 |
NC_000003.10:g.170965375T>A | NCBI36 |
NG_016363.1:g.5168A>T , LRG_347:g.5168A>T |
HGVS | Amino-acid change | |
---|---|---|
NR_001566.1:n.168A>T , LRG_347t1:n.168A>T |