HGVS | Genome Assembly |
---|---|
NC_000007.14:g.41772195T>A , CM000669.2:g.41772195T>A | GRCh38 |
NC_000007.13:g.41811793T>A , CM000669.1:g.41811793T>A | GRCh37 |
NC_000007.12:g.41778318T>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
NR_027118.1:n.359-701T>A | ||
NR_027118.2:n.356-701T>A | ||
XR_001745185.1:n.964+36481T>A | ||
XR_001745186.1:n.954+36491T>A |