HGVS | Genome Assembly |
---|---|
NC_000008.11:g.16992799del , CM000670.2:g.16992799del | GRCh38 |
NC_000008.10:g.16850308del , CM000670.1:g.16850308del | GRCh37 |
NC_000008.9:g.16894679del | NCBI36 |
NG_015978.1:g.14368del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000180166.6:c.*274del MANE Select | ENSP00000180166.5:n.*274del | |
ENST00000180166.5:c.*274del | ENSP00000180166.5:n.*274del | |
NM_019851.3:c.*274del MANE Select | NP_062825.1:n.*274del |