HGVS | Genome Assembly |
---|---|
NC_000012.12:g.110717824T>A , CM000674.2:g.110717824T>A | GRCh38 |
NC_000012.11:g.111155629T>A , CM000674.1:g.111155629T>A | GRCh37 |
NC_000012.10:g.109640012T>A | NCBI36 |
NG_030325.1:g.30155A>T |
HGVS | Amino-acid Change | |
---|---|---|
XM_011538504.1:c.944-2677A>T | XP_011536806.1:n.944-2677A>T | |
XM_011538505.1:c.943+3281A>T | XP_011536807.1:n.943+3281A>T | |
XM_011538504.3:c.944-2677A>T | XP_011536806.1:n.944-2677A>T | |
XM_011538505.3:c.943+3281A>T | XP_011536807.1:n.943+3281A>T |