HGVS | Genome Assembly |
---|---|
NC_000012.12:g.6470990C>T , CM000674.2:g.6470990C>T | GRCh38 |
NC_000012.11:g.6580156C>T , CM000674.1:g.6580156C>T | GRCh37 |
NC_000012.10:g.6450417C>T | NCBI36 |
NG_042188.1:g.4910G>A | |
NG_042188.2:g.4910G>A |
HGVS | Amino-acid Change | |
---|---|---|
XR_001748777.2:n.2257C>T | ||
XR_001748778.2:n.2254C>T |