HGVS | Genome Assembly |
---|---|
NC_000012.12:g.110717653C>T , CM000674.2:g.110717653C>T | GRCh38 |
NC_000012.11:g.111155458C>T , CM000674.1:g.111155458C>T | GRCh37 |
NC_000012.10:g.109639841C>T | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
XM_011538504.1:c.944-2506G>A | XP_011536806.1:n.944-2506G>A | |
XM_011538505.1:c.943+3452G>A | XP_011536807.1:n.943+3452G>A | |
XM_011538504.3:c.944-2506G>A | XP_011536806.1:n.944-2506G>A | |
XM_011538505.3:c.943+3452G>A | XP_011536807.1:n.943+3452G>A |