HGVS | Genome Assembly |
---|---|
NC_000010.11:g.122461591_122461603dup , CM000672.2:g.122461591_122461603dup | GRCh38 |
NC_000010.10:g.124221107_124221119dup , CM000672.1:g.124221107_124221119dup | GRCh37 |
NC_000010.9:g.124211097_124211109dup | NCBI36 |
NG_011554.1:g.5067_5079dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368984.8:c.-62_-50dup MANE Select | ENSP00000357980.3:n.-62_-50dup | |
ENST00000648167.1:c.154+2882_154+2894dup | ENSP00000498033.1:n.154+2882_154+2894dup | |
ENST00000368984.7:c.-62_-50dup | ENSP00000357980.3:n.-62_-50dup | |
NM_002775.4:c.-62_-50dup | NP_002766.1:n.-62_-50dup | |
NM_002775.5:c.-62_-50dup MANE Select | NP_002766.1:n.-62_-50dup |