HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52516686C>A , CM000674.2:g.52516686C>A | GRCh38 |
NC_000012.11:g.52910470C>A , CM000674.1:g.52910470C>A | GRCh37 |
NC_000012.10:g.51196737C>A | NCBI36 |
NG_008297.1:g.8774G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252242.9:c.1390G>T MANE Select | ENSP00000252242.4:p.Asp464Tyr | |
ENST00000252242.8:c.1390G>T | ENSP00000252242.4:p.Asp464Tyr | |
ENST00000548409.5:c.512G>T | ||
ENST00000549511.5:n.597G>T | ||
ENST00000552629.5:n.1488G>T | ||
NM_000424.3:c.1390G>T | NP_000415.2:p.Asp464Tyr | |
NM_000424.4:c.1390G>T MANE Select | NP_000415.2:p.Asp464Tyr |