HGVS | Genome Assembly |
---|---|
NC_000007.14:g.41772164T>G , CM000669.2:g.41772164T>G | GRCh38 |
NC_000007.13:g.41811762T>G , CM000669.1:g.41811762T>G | GRCh37 |
NC_000007.12:g.41778287T>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
NR_027118.1:n.359-732T>G | ||
NR_027118.2:n.356-732T>G | ||
XR_001745185.1:n.964+36450T>G | ||
XR_001745186.1:n.954+36460T>G |