HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32390436T>C , CM000668.2:g.32390436T>C | GRCh38 |
NC_000006.11:g.32358213T>C , CM000668.1:g.32358213T>C | GRCh37 |
NC_000006.10:g.32466191T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
XM_011515039.1:c.482-15018T>C | XP_011513341.1:n.482-15018T>C | |
NR_136245.1:n.303-15018T>C |