HGVS | Genome Assembly |
---|---|
NC_000010.11:g.122496899G= , CM000672.2:g.122496899G= | GRCh38 |
NC_000010.10:g.124256415G= , CM000672.1:g.124256415G= | GRCh37 |
NC_000010.9:g.124246405G= | NCBI36 |
NG_011554.1:g.40375G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000368984.8:c.777+7273G= MANE Select | ENSP00000357980.3:n.777+7273G= | |
ENST00000648167.1:c.459+7273G= | ENSP00000498033.1:n.459+7273G= | |
ENST00000368984.7:c.777+7273G= | ENSP00000357980.3:n.777+7273G= | |
NM_002775.4:c.777+7273G= | NP_002766.1:n.777+7273G= | |
NM_002775.5:c.777+7273G= MANE Select | NP_002766.1:n.777+7273G= |