HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94021484_94021485insA , CM000663.2:g.94021484_94021485insA | GRCh38 |
NC_000001.10:g.94487040_94487041insA , CM000663.1:g.94487040_94487041insA | GRCh37 |
NC_000001.9:g.94259628_94259629insA | NCBI36 |
NG_009073.1:g.104665_104666insT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.4849-76_4849-75insT MANE Select | ENSP00000359245.3:n.4849-76_4849-75insT | |
ENST00000370225.3:c.4849-76_4849-75insT | ENSP00000359245.3:n.4849-76_4849-75insT | |
ENST00000460514.1:n.343-76_343-75insT | ||
ENST00000536513.5:c.1225-76_1225-75insT | ENSP00000439707.2:n.1225-76_1225-75insT | |
NM_000350.2:c.4849-76_4849-75insT | NP_000341.2:n.4849-76_4849-75insT | |
NM_000350.3:c.4849-76_4849-75insT MANE Select | NP_000341.2:n.4849-76_4849-75insT |