HGVS | Genome Assembly |
---|---|
NC_000015.10:g.74755379_74755380del , CM000677.2:g.74755379_74755380del | GRCh38 |
NC_000015.9:g.75047720_75047721del , CM000677.1:g.75047720_75047721del | GRCh37 |
NC_000015.8:g.72834773_72834774del | NCBI36 |
NG_008431.1:g.37838_37839del | |
NG_008431.2:g.37838_37839del | |
NG_061543.1:g.11535_11536del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000343932.5:c.*291_*292del MANE Select | ENSP00000342007.4:n.*291_*292del | |
ENST00000343932.4:c.*291_*292del | ENSP00000342007.4:n.*291_*292del | |
NM_000761.4:c.*291_*292del | NP_000752.2:n.*291_*292del | |
NM_000761.5:c.*291_*292del MANE Select | NP_000752.2:n.*291_*292del |