HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41586859_41586861del , CM000679.2:g.41586859_41586861del | GRCh38 |
NC_000017.10:g.39743111_39743113del , CM000679.1:g.39743111_39743113del | GRCh37 |
NC_000017.9:g.36996637_36996639del | NCBI36 |
NG_008624.1:g.5035_5037del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000167586.7:c.-27_-25del MANE Select | ENSP00000167586.6:n.-27_-25del | |
ENST00000167586.6:c.-27_-25del | ENSP00000167586.6:n.-27_-25del | |
NM_000526.4:c.-27_-25del | NP_000517.2:n.-27_-25del | |
NM_000526.5:c.-27_-25del MANE Select | NP_000517.3:n.-27_-25del |