HGVS | Genome Assembly |
---|---|
NC_000012.12:g.110717297T>C , CM000674.2:g.110717297T>C | GRCh38 |
NC_000012.11:g.111155102T>C , CM000674.1:g.111155102T>C | GRCh37 |
NC_000012.10:g.109639485T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
XM_011538504.1:c.944-2150A>G | XP_011536806.1:n.944-2150A>G | |
XM_011538505.1:c.943+3808A>G | XP_011536807.1:n.943+3808A>G | |
XM_011538504.3:c.944-2150A>G | XP_011536806.1:n.944-2150A>G | |
XM_011538505.3:c.943+3808A>G | XP_011536807.1:n.943+3808A>G |