HGVS | Genome Assembly |
---|---|
NC_000001.11:g.149884939A= , CM000663.2:g.149884939A= | GRCh38 |
NC_000001.10:g.149856489A= , CM000663.1:g.149856489A= | GRCh37 |
NC_000001.9:g.148123113A= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369155.4:c.*1321T= MANE Select | ENSP00000358151.2:n.*1321T= | |
ENST00000369155.3:c.*1321T= | ENSP00000358151.2:n.*1321T= | |
ENST00000369160.3:c.377+1325T= | ENSP00000375736.2:n.377+1325T= | |
NM_003528.2:c.*1321T= | NP_003519.1:n.*1321T= | |
NM_003528.3:c.*1321T= MANE Select | NP_003519.1:n.*1321T= |