HGVS | Genome Assembly |
---|---|
NC_000012.12:g.76345788T= , CM000674.2:g.76345788T= | GRCh38 |
NC_000012.11:g.76739568T= , CM000674.1:g.76739568T= | GRCh37 |
NC_000012.10:g.75263699T= | NCBI36 |
NG_016357.1:g.7655A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000650064.2:c.*25A= MANE Select | ENSP00000497413.1:n.*25A= | |
ENST00000393262.3:c.*25A= | ENSP00000376946.3:n.*25A= | |
NM_024685.3:c.*25A= | NP_078961.3:n.*25A= | |
NM_024685.4:c.*25A= MANE Select | NP_078961.3:n.*25A= |