HGVS | Genome Assembly |
---|---|
NC_000007.14:g.41772190A>T , CM000669.2:g.41772190A>T | GRCh38 |
NC_000007.13:g.41811788A>T , CM000669.1:g.41811788A>T | GRCh37 |
NC_000007.12:g.41778313A>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
NR_027118.1:n.359-706A>T | ||
NR_027118.2:n.356-706A>T | ||
XR_001745185.1:n.964+36476A>T | ||
XR_001745186.1:n.954+36486A>T |