HGVS | Genome Assembly |
---|---|
NC_000010.11:g.122496892A= , CM000672.2:g.122496892A= | GRCh38 |
NC_000010.10:g.124256408A= , CM000672.1:g.124256408A= | GRCh37 |
NC_000010.9:g.124246398A= | NCBI36 |
NG_011554.1:g.40368A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000368984.8:c.777+7266A= MANE Select | ENSP00000357980.3:n.777+7266A= | |
ENST00000648167.1:c.459+7266A= | ENSP00000498033.1:n.459+7266A= | |
ENST00000368984.7:c.777+7266A= | ENSP00000357980.3:n.777+7266A= | |
NM_002775.4:c.777+7266A= | NP_002766.1:n.777+7266A= | |
NM_002775.5:c.777+7266A= MANE Select | NP_002766.1:n.777+7266A= |