HGVS | Genome Assembly |
---|---|
NC_000006.12:g.10886716C>A , CM000668.2:g.10886716C>A | GRCh38 |
NC_000006.11:g.10886949C>A , CM000668.1:g.10886949C>A | GRCh37 |
NC_000006.10:g.10994935C>A | NCBI36 |
NG_008970.1:g.150G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000480294.1:c.101-4797C>A | ENSP00000417929.1:n.101-4797C>A |