HGVS | Genome Assembly |
---|---|
NC_000012.12:g.110717865T>C , CM000674.2:g.110717865T>C | GRCh38 |
NC_000012.11:g.111155670T>C , CM000674.1:g.111155670T>C | GRCh37 |
NC_000012.10:g.109640053T>C | NCBI36 |
NG_030325.1:g.30114A>G |
HGVS | Amino-acid Change | |
---|---|---|
XM_011538504.1:c.944-2718A>G | XP_011536806.1:n.944-2718A>G | |
XM_011538505.1:c.943+3240A>G | XP_011536807.1:n.943+3240A>G | |
XM_011538504.3:c.944-2718A>G | XP_011536806.1:n.944-2718A>G | |
XM_011538505.3:c.943+3240A>G | XP_011536807.1:n.943+3240A>G |