HGVS | Genome Assembly |
---|---|
NC_000012.12:g.65964417T= , CM000674.2:g.65964417T= | GRCh38 |
NC_000012.11:g.66358197T= , CM000674.1:g.66358197T= | GRCh37 |
NC_000012.10:g.64644464T= | NCBI36 |
NG_016296.1:g.144958T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000403681.7:c.*1125T= MANE Select | ENSP00000384026.2:n.*1125T= | |
ENST00000403681.6:c.*1125T= | ENSP00000384026.2:n.*1125T= | |
NM_003483.4:c.*1125T= | NP_003474.1:n.*1125T= | |
NM_003483.6:c.*1125T= MANE Select | NP_003474.1:n.*1125T= |