HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17401555T>G , CM000663.2:g.17401555T>G | GRCh38 |
NC_000001.10:g.17728051T>G , CM000663.1:g.17728051T>G | GRCh37 |
NC_000001.9:g.17600638T>G | NCBI36 |
NG_032943.1:g.34310T>G | |
NG_032943.2:g.34310T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000619609.1:c.*117T>G MANE Select | ENSP00000483125.1:n.*117T>G | |
NM_207421.4:c.*117T>G MANE Select | NP_997304.3:n.*117T>G |