HGVS | Genome Assembly |
---|---|
NC_000002.12:g.118079695C>T , CM000664.2:g.118079695C>T | GRCh38 |
NC_000002.11:g.118837271C>T , CM000664.1:g.118837271C>T | GRCh37 |
NC_000002.10:g.118553741C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
XM_011512305.1:c.697-2163G>A | XP_011510607.1:n.697-2163G>A | |
XR_001739662.2:n.138+8556G>A |