HGVS | Genome Assembly |
---|---|
NC_000007.14:g.41772187A>C , CM000669.2:g.41772187A>C | GRCh38 |
NC_000007.13:g.41811785A>C , CM000669.1:g.41811785A>C | GRCh37 |
NC_000007.12:g.41778310A>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
NR_027118.1:n.359-709A>C | ||
NR_027118.2:n.356-709A>C | ||
XR_001745185.1:n.964+36473A>C | ||
XR_001745186.1:n.954+36483A>C |