HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52516346T>A , CM000674.2:g.52516346T>A | GRCh38 |
NC_000012.11:g.52910130T>A , CM000674.1:g.52910130T>A | GRCh37 |
NC_000012.10:g.51196397T>A | NCBI36 |
NG_008297.1:g.9114A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252242.9:c.1439+291A>T MANE Select | ENSP00000252242.4:n.1439+291A>T | |
ENST00000252242.8:c.1439+291A>T | ENSP00000252242.4:n.1439+291A>T | |
ENST00000548409.5:c.561+291A>T | ||
ENST00000549511.5:n.646+291A>T | ||
ENST00000552629.5:n.1828A>T | ||
NM_000424.3:c.1439+291A>T | NP_000415.2:n.1439+291A>T | |
NM_000424.4:c.1439+291A>T MANE Select | NP_000415.2:n.1439+291A>T |