HGVS | Genome Assembly |
---|---|
NC_000010.11:g.93601750T>A , CM000672.2:g.93601750T>A | GRCh38 |
NC_000010.10:g.95361507T>A , CM000672.1:g.95361507T>A | GRCh37 |
NC_000010.9:g.95351497T>A | NCBI36 |
NG_009104.1:g.4487A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000604414.1:c.697-2324T>A | ENSP00000474477.1:n.697-2324T>A |