HGVS | Genome Assembly |
---|---|
NC_000012.12:g.110717877A>C , CM000674.2:g.110717877A>C | GRCh38 |
NC_000012.11:g.111155682A>C , CM000674.1:g.111155682A>C | GRCh37 |
NC_000012.10:g.109640065A>C | NCBI36 |
NG_030325.1:g.30102T>G |
HGVS | Amino-acid Change | |
---|---|---|
XM_011538504.1:c.944-2730T>G | XP_011536806.1:n.944-2730T>G | |
XM_011538505.1:c.943+3228T>G | XP_011536807.1:n.943+3228T>G | |
XM_011538504.3:c.944-2730T>G | XP_011536806.1:n.944-2730T>G | |
XM_011538505.3:c.943+3228T>G | XP_011536807.1:n.943+3228T>G |