HGVS | Genome Assembly |
---|---|
NC_000011.10:g.640251_640268dup , CM000673.2:g.640251_640268dup | GRCh38 |
NC_000011.9:g.640251_640268dup , CM000673.1:g.640251_640268dup | GRCh37 |
NC_000011.8:g.630251_630268dup | NCBI36 |
NG_021241.1:g.7947_7964dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000176183.6:c.1002_1019dup MANE Select | ENSP00000176183.5:p.Arg340_Glu341insAlaLy... | |
ENST00000176183.5:c.1002_1019dup | ENSP00000176183.5:p.Arg340_Glu341insAlaLy... | |
NM_000797.3:c.1002_1019dup | NP_000788.2:p.Arg340_Glu341insAlaLysIleTh... | |
NM_000797.4:c.1002_1019dup MANE Select | NP_000788.2:p.Arg340_Glu341insAlaLysIleTh... |