HGVS | Genome Assembly |
---|---|
NC_000007.14:g.155463223del , CM000669.2:g.155463223del | GRCh38 |
NC_000007.13:g.155255918del , CM000669.1:g.155255918del | GRCh37 |
NC_000007.12:g.154948679del | NCBI36 |
NG_007124.1:g.11504del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000297375.4:c.*536del MANE Select | ENSP00000297375.4:n.*536del | |
NM_001427.3:c.*536del | NP_001418.2:n.*536del | |
NM_001427.4:c.*536del MANE Select | NP_001418.2:n.*536del |