HGVS | Genome Assembly |
---|---|
NC_000013.11:g.53051585_53051593del , CM000675.2:g.53051585_53051593del | GRCh38 |
NC_000013.10:g.53625720_53625728del , CM000675.1:g.53625720_53625728del | GRCh37 |
NC_000013.9:g.52523721_52523729del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000219022.3:c.*814_*822del MANE Select | ENSP00000219022.2:n.*814_*822del | |
ENST00000219022.2:c.*814_*822del | ENSP00000219022.2:n.*814_*822del | |
NM_006418.4:c.*814_*822del | NP_006409.3:n.*814_*822del | |
NM_006418.5:c.*814_*822del MANE Select | NP_006409.3:n.*814_*822del |