HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94021507_94021514del , CM000663.2:g.94021507_94021514del | GRCh38 |
NC_000001.10:g.94487063_94487070del , CM000663.1:g.94487063_94487070del | GRCh37 |
NC_000001.9:g.94259651_94259658del | NCBI36 |
NG_009073.1:g.104636_104643del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.4849-105_4849-98del MANE Select | ENSP00000359245.3:n.4849-105_4849-98del | |
ENST00000370225.3:c.4849-105_4849-98del | ENSP00000359245.3:n.4849-105_4849-98del | |
ENST00000460514.1:n.343-105_343-98del | ||
ENST00000536513.5:c.1225-105_1225-98del | ENSP00000439707.2:n.1225-105_1225-98del | |
NM_000350.2:c.4849-105_4849-98del | NP_000341.2:n.4849-105_4849-98del | |
NM_000350.3:c.4849-105_4849-98del MANE Select | NP_000341.2:n.4849-105_4849-98del |