HGVS | Genome Assembly |
---|---|
NC_000007.14:g.41782319C>T , CM000669.2:g.41782319C>T | GRCh38 |
NC_000007.13:g.41821917C>T , CM000669.1:g.41821917C>T | GRCh37 |
NC_000007.12:g.41788442C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
XR_001745185.1:n.964+46605C>T | ||
XR_001745186.1:n.954+46615C>T |