HGVS | Genome Assembly |
---|---|
NC_000007.14:g.41772171T>C , CM000669.2:g.41772171T>C | GRCh38 |
NC_000007.13:g.41811769T>C , CM000669.1:g.41811769T>C | GRCh37 |
NC_000007.12:g.41778294T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
NR_027118.1:n.359-725T>C | ||
NR_027118.2:n.356-725T>C | ||
XR_001745185.1:n.964+36457T>C | ||
XR_001745186.1:n.954+36467T>C |