HGVS | Genome Assembly |
---|---|
NC_000001.11:g.149928322C>A , CM000663.2:g.149928322C>A | GRCh38 |
NC_000001.10:g.149900214C>A , CM000663.1:g.149900214C>A | GRCh37 |
NC_000001.9:g.148166838C>A | NCBI36 |
NG_032777.1:g.4931G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000271628.8:c.-563G>T | ENSP00000271628.8:n.-563G>T |