HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94007541_94007565del , CM000663.2:g.94007541_94007565del | GRCh38 |
NC_000001.10:g.94473097_94473121del , CM000663.1:g.94473097_94473121del | GRCh37 |
NC_000001.9:g.94245685_94245709del | NCBI36 |
NG_009073.1:g.118587_118611del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.6005+71_6005+95del MANE Select | ENSP00000359245.3:n.6005+71_6005+95del | |
ENST00000370225.3:c.6005+71_6005+95del | ENSP00000359245.3:n.6005+71_6005+95del | |
ENST00000465352.1:n.421+71_421+95del | ||
ENST00000484388.1:n.119+71_119+95del | ||
ENST00000536513.5:c.2381+71_2381+95del | ENSP00000439707.2:n.2381+71_2381+95del | |
NM_000350.2:c.6005+71_6005+95del | NP_000341.2:n.6005+71_6005+95del | |
NM_000350.3:c.6005+71_6005+95del MANE Select | NP_000341.2:n.6005+71_6005+95del |