HGVS | Genome Assembly |
---|---|
NC_000023.11:g.108084805T= , CM000685.2:g.108084805T= | GRCh38 |
NC_000023.10:g.107328035T= , CM000685.1:g.107328035T= | GRCh37 |
NC_000023.9:g.107214691T= | NCBI36 |
NG_012521.1:g.11814A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000217958.8:c.*169A= MANE Select | ENSP00000217958.3:n.*169A= | |
ENST00000217958.7:c.*169A= | ENSP00000217958.3:n.*169A= | |
ENST00000372295.5:c.*169A= | ENSP00000361369.1:n.*169A= | |
ENST00000372296.5:c.*315A= | ENSP00000361370.1:n.*315A= | |
NM_002814.3:c.*169A= | NP_002805.1:n.*169A= | |
NM_170750.2:c.*315A= | NP_736606.1:n.*315A= | |
NM_002814.4:c.*169A= MANE Select | NP_002805.1:n.*169A= | |
NM_170750.3:c.*315A= | NP_736606.1:n.*315A= |