HGVS | Genome Assembly |
---|---|
NC_000012.12:g.110717857A>G , CM000674.2:g.110717857A>G | GRCh38 |
NC_000012.11:g.111155662A>G , CM000674.1:g.111155662A>G | GRCh37 |
NC_000012.10:g.109640045A>G | NCBI36 |
NG_030325.1:g.30122T>C |
HGVS | Amino-acid Change | |
---|---|---|
XM_011538504.1:c.944-2710T>C | XP_011536806.1:n.944-2710T>C | |
XM_011538505.1:c.943+3248T>C | XP_011536807.1:n.943+3248T>C | |
XM_011538504.3:c.944-2710T>C | XP_011536806.1:n.944-2710T>C | |
XM_011538505.3:c.943+3248T>C | XP_011536807.1:n.943+3248T>C |