HGVS | Genome Assembly |
---|---|
NC_000012.12:g.114670363A= , CM000674.2:g.114670363A= | GRCh38 |
NC_000012.11:g.115108168A= , CM000674.1:g.115108168A= | GRCh37 |
NC_000012.10:g.113592551A= | NCBI36 |
NG_008315.1:g.18802T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000349155.7:c.*1478T= MANE Select | ENSP00000257567.2:n.*1478T= | |
ENST00000257566.7:c.*1478T= | ENSP00000257566.3:n.*1478T= | |
ENST00000349155.6:c.*1478T= | ENSP00000257567.2:n.*1478T= | |
NM_005996.3:c.*1478T= | NP_005987.3:n.*1478T= | |
NM_016569.3:c.*1478T= | NP_057653.3:n.*1478T= | |
NM_005996.4:c.*1478T= MANE Select | NP_005987.3:n.*1478T= | |
NM_016569.4:c.*1478T= | NP_057653.3:n.*1478T= |