HGVS | Genome Assembly |
---|---|
NC_000015.10:g.74755350del , CM000677.2:g.74755350del | GRCh38 |
NC_000015.9:g.75047691del , CM000677.1:g.75047691del | GRCh37 |
NC_000015.8:g.72834744del | NCBI36 |
NG_008431.1:g.37809del | |
NG_008431.2:g.37809del | |
NG_061543.1:g.11506del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000343932.5:c.*262del MANE Select | ENSP00000342007.4:n.*262del | |
ENST00000343932.4:c.*262del | ENSP00000342007.4:n.*262del | |
NM_000761.4:c.*262del | NP_000752.2:n.*262del | |
NM_000761.5:c.*262del MANE Select | NP_000752.2:n.*262del |