HGVS | Genome Assembly |
---|---|
NC_000001.11:g.149884432C>A , CM000663.2:g.149884432C>A | GRCh38 |
NC_000001.10:g.149855982C>A , CM000663.1:g.149855982C>A | GRCh37 |
NC_000001.9:g.148122606C>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369160.3:c.377+1832G>T | ENSP00000375736.2:n.377+1832G>T |