HGVS | Genome Assembly |
---|---|
NC_000004.12:g.4863169del , CM000666.2:g.4863169del | GRCh38 |
NC_000004.11:g.4864896del , CM000666.1:g.4864896del | GRCh37 |
NC_000004.10:g.4915797del | NCBI36 |
NG_008121.1:g.8505del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382723.5:c.*26del MANE Select | ENSP00000372170.4:n.*26del | |
ENST00000382723.4:c.*26del | ENSP00000372170.4:n.*26del | |
NM_002448.3:c.*26del MANE Select | NP_002439.2:n.*26del |