HGVS | Genome Assembly |
---|---|
NC_000014.9:g.75985689G>T , CM000676.2:g.75985689G>T | GRCh38 |
NC_000014.8:g.76452032G>T , CM000676.1:g.76452032G>T | GRCh37 |
NC_000014.7:g.75521785G>T | NCBI36 |
NG_011715.1:g.1061C>A , LRG_399:g.1061C>A | |
NG_031957.1:g.4937G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000555677.5:n.90-3196G>T |