HGVS | Genome Assembly |
---|---|
NC_000012.12:g.47908701C>A , CM000674.2:g.47908701C>A | GRCh38 |
NC_000012.11:g.48302484C>A , CM000674.1:g.48302484C>A | GRCh37 |
NC_000012.10:g.46588751C>A | NCBI36 |
NG_008731.1:g.1331G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000395324.6:c.-83-25927G>T | ENSP00000378734.2:n.-83-25927G>T |