HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52652148del , CM000674.2:g.52652148del | GRCh38 |
NC_000012.11:g.53045932del , CM000674.1:g.53045932del | GRCh37 |
NC_000012.10:g.51332199del | NCBI36 |
NG_008296.1:g.5029del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000309680.4:c.-5del MANE Select | ENSP00000310861.3:n.-5del | |
ENST00000309680.3:c.-5del | ENSP00000310861.3:n.-5del | |
NM_000423.2:c.-5del | NP_000414.2:n.-5del | |
NM_000423.3:c.-5del MANE Select | NP_000414.2:n.-5del |