HGVS | Genome Assembly |
---|---|
NC_000013.11:g.53051653A>T , CM000675.2:g.53051653A>T | GRCh38 |
NC_000013.10:g.53625788A>T , CM000675.1:g.53625788A>T | GRCh37 |
NC_000013.9:g.52523789A>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000219022.3:c.*882A>T MANE Select | ENSP00000219022.2:n.*882A>T | |
ENST00000219022.2:c.*882A>T | ENSP00000219022.2:n.*882A>T | |
NM_006418.4:c.*882A>T | NP_006409.3:n.*882A>T | |
NM_006418.5:c.*882A>T MANE Select | NP_006409.3:n.*882A>T |