HGVS | Genome Assembly |
---|---|
NC_000010.11:g.93601756T>G , CM000672.2:g.93601756T>G | GRCh38 |
NC_000010.10:g.95361513T>G , CM000672.1:g.95361513T>G | GRCh37 |
NC_000010.9:g.95351503T>G | NCBI36 |
NG_009104.1:g.4481A>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000604414.1:c.697-2318T>G | ENSP00000474477.1:n.697-2318T>G |