HGVS | Genome Assembly |
---|---|
NC_000014.9:g.75985687C>T , CM000676.2:g.75985687C>T | GRCh38 |
NC_000014.8:g.76452030C>T , CM000676.1:g.76452030C>T | GRCh37 |
NC_000014.7:g.75521783C>T | NCBI36 |
NG_011715.1:g.1063G>A , LRG_399:g.1063G>A | |
NG_031957.1:g.4935C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000555677.5:n.90-3198C>T |