HGVS | Genome Assembly |
---|---|
NC_000014.9:g.75985698T>C , CM000676.2:g.75985698T>C | GRCh38 |
NC_000014.8:g.76452041T>C , CM000676.1:g.76452041T>C | GRCh37 |
NC_000014.7:g.75521794T>C | NCBI36 |
NG_011715.1:g.1052A>G , LRG_399:g.1052A>G | |
NG_031957.1:g.4946T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000555677.5:n.90-3187T>C |