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