HGVS | Genome Assembly |
---|---|
NC_000012.12:g.65964499T= , CM000674.2:g.65964499T= | GRCh38 |
NC_000012.11:g.66358279T= , CM000674.1:g.66358279T= | GRCh37 |
NC_000012.10:g.64644546T= | NCBI36 |
NG_016296.1:g.145040T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000403681.7:c.*1207T= MANE Select | ENSP00000384026.2:n.*1207T= | |
ENST00000403681.6:c.*1207T= | ENSP00000384026.2:n.*1207T= | |
NM_003483.4:c.*1207T= | NP_003474.1:n.*1207T= | |
NM_003483.6:c.*1207T= MANE Select | NP_003474.1:n.*1207T= |