HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41586912C>A , CM000679.2:g.41586912C>A | GRCh38 |
NC_000017.10:g.39743164C>A , CM000679.1:g.39743164C>A | GRCh37 |
NC_000017.9:g.36996690C>A | NCBI36 |
NG_008624.1:g.4984G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000167586.6:c.-78G>T | ENSP00000167586.6:n.-78G>T |