HGVS | Genome Assembly |
---|---|
NC_000014.9:g.75985696C>A , CM000676.2:g.75985696C>A | GRCh38 |
NC_000014.8:g.76452039C>A , CM000676.1:g.76452039C>A | GRCh37 |
NC_000014.7:g.75521792C>A | NCBI36 |
NG_011715.1:g.1054G>T , LRG_399:g.1054G>T | |
NG_031957.1:g.4944C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000555677.5:n.90-3189C>A |