HGVS | Genome Assembly |
---|---|
NC_000007.14:g.41772327A>G , CM000669.2:g.41772327A>G | GRCh38 |
NC_000007.13:g.41811925A>G , CM000669.1:g.41811925A>G | GRCh37 |
NC_000007.12:g.41778450A>G | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
NR_027118.1:n.359-569A>G | ||
NR_027118.2:n.356-569A>G | ||
XR_001745185.1:n.964+36613A>G | ||
XR_001745186.1:n.954+36623A>G |