HGVS | Genome Assembly |
---|---|
NC_000023.11:g.43949723dup , CM000685.2:g.43949723dup | GRCh38 |
NC_000023.10:g.43808969dup , CM000685.1:g.43808969dup | GRCh37 |
NC_000023.9:g.43693913dup | NCBI36 |
NG_009832.1:g.28956dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000642620.1:c.*79dup MANE Select | ENSP00000495972.1:n.*79dup | |
ENST00000647044.1:c.*79dup | ENSP00000495811.1:n.*79dup | |
ENST00000378062.5:c.*79dup | ENSP00000367301.5:n.*79dup | |
ENST00000470584.1:n.525dup | ||
NM_000266.3:c.*79dup | NP_000257.1:n.*79dup | |
NM_000266.4:c.*79dup MANE Select | NP_000257.1:n.*79dup |