HGVS | Genome Assembly |
---|---|
NC_000003.12:g.169764647C>T , CM000665.2:g.169764647C>T | GRCh38 |
NC_000003.11:g.169482435C>T , CM000665.1:g.169482435C>T | GRCh37 |
NC_000003.10:g.170965129C>T | NCBI36 |
NG_016363.1:g.5414G>A , LRG_347:g.5414G>A |
HGVS | Amino-acid Change | |
---|---|---|
NR_001566.1:n.414G>A , LRG_347t1:n.414G>A |