HGVS | Genome Assembly |
---|---|
NC_000005.10:g.45462119dup , CM000667.2:g.45462119dup | GRCh38 |
NC_000005.9:g.45462221dup , CM000667.1:g.45462221dup | GRCh37 |
NC_000005.8:g.45497978dup | NCBI36 |
NG_042183.1:g.239004dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000303230.6:c.850-108dup MANE Select | ENSP00000307342.4:n.850-108dup | |
ENST00000637305.1:n.13-108dup | ||
ENST00000673735.1:c.850-108dup | ENSP00000501107.1:n.850-108dup | |
ENST00000303230.5:c.850-108dup | ENSP00000307342.4:n.850-108dup | |
NM_021072.3:c.850-108dup | NP_066550.2:n.850-108dup | |
NM_021072.4:c.850-108dup MANE Select | NP_066550.2:n.850-108dup |