HGVS | Genome Assembly |
---|---|
NC_000001.11:g.155290174T>C , CM000663.2:g.155290174T>C | GRCh38 |
NC_000001.10:g.155259965T>C , CM000663.1:g.155259965T>C | GRCh37 |
NC_000001.9:g.153526589T>C | NCBI36 |
NG_011677.1:g.16261A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000342741.6:c.*398A>G MANE Select | ENSP00000339933.4:n.*398A>G | |
ENST00000392414.7:c.*398A>G | ENSP00000376214.3:n.*398A>G | |
NM_000298.5:c.*398A>G | NP_000289.1:n.*398A>G | |
NM_181871.3:c.*398A>G | NP_870986.1:n.*398A>G | |
NM_000298.6:c.*398A>G MANE Select | NP_000289.1:n.*398A>G | |
NM_181871.4:c.*398A>G | NP_870986.1:n.*398A>G |