HGVS | Genome Assembly |
---|---|
NC_000012.12:g.6470980T>A , CM000674.2:g.6470980T>A | GRCh38 |
NC_000012.11:g.6580146T>A , CM000674.1:g.6580146T>A | GRCh37 |
NC_000012.10:g.6450407T>A | NCBI36 |
NG_042188.1:g.4920A>T | |
NG_042188.2:g.4920A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361716.7:c.-449A>T (VAMP1) | ENSP00000355122.3:n.-449A>T | |
XR_001748777.2:n.2247T>A (TAPBPL) | ||
XR_001748778.2:n.2244T>A (TAPBPL) |