HGVS | Genome Assembly |
---|---|
NC_000010.11:g.122507170G>T , CM000672.2:g.122507170G>T | GRCh38 |
NC_000010.10:g.124266686G>T , CM000672.1:g.124266686G>T | GRCh37 |
NC_000010.9:g.124256676G>T | NCBI36 |
NG_011554.1:g.50646G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368984.8:c.973-200G>T MANE Select | ENSP00000357980.3:n.973-200G>T | |
ENST00000648167.1:c.655-200G>T | ENSP00000498033.1:n.655-200G>T | |
ENST00000368984.7:c.973-200G>T | ENSP00000357980.3:n.973-200G>T | |
ENST00000420892.1:c.196-200G>T | ENSP00000412676.1:n.196-200G>T | |
NM_002775.4:c.973-200G>T | NP_002766.1:n.973-200G>T | |
NM_002775.5:c.973-200G>T MANE Select | NP_002766.1:n.973-200G>T |