HGVS | Genome Assembly |
---|---|
NC_000010.11:g.93601764G>A , CM000672.2:g.93601764G>A | GRCh38 |
NC_000010.10:g.95361521G>A , CM000672.1:g.95361521G>A | GRCh37 |
NC_000010.9:g.95351511G>A | NCBI36 |
NG_009104.1:g.4473C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000604414.1:c.697-2310G>A | ENSP00000474477.1:n.697-2310G>A |