HGVS | Genome Assembly |
---|---|
NC_000011.10:g.116822836del , CM000673.2:g.116822836del | GRCh38 |
NC_000011.9:g.116693552del , CM000673.1:g.116693552del | GRCh37 |
NC_000011.8:g.116198762del | NCBI36 |
NG_012044.1:g.5463del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000357780.5:c.50-48del MANE Select | ENSP00000350425.3:n.50-48del | |
ENST00000357780.4:c.50-48del | ENSP00000350425.3:n.50-48del | |
NM_000482.3:c.50-48del | NP_000473.2:n.50-48del | |
NM_000482.4:c.50-48del MANE Select | NP_000473.2:n.50-48del |