HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17401479G>A , CM000663.2:g.17401479G>A | GRCh38 |
NC_000001.10:g.17727975G>A , CM000663.1:g.17727975G>A | GRCh37 |
NC_000001.9:g.17600562G>A | NCBI36 |
NG_032943.1:g.34234G>A | |
NG_032943.2:g.34234G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000619609.1:c.*41G>A MANE Select | ENSP00000483125.1:n.*41G>A | |
NM_207421.4:c.*41G>A MANE Select | NP_997304.3:n.*41G>A |