HGVS | Genome Assembly |
---|---|
NC_000010.11:g.93601751T>C , CM000672.2:g.93601751T>C | GRCh38 |
NC_000010.10:g.95361508T>C , CM000672.1:g.95361508T>C | GRCh37 |
NC_000010.9:g.95351498T>C | NCBI36 |
NG_009104.1:g.4486A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000604414.1:c.697-2323T>C | ENSP00000474477.1:n.697-2323T>C |