HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52516720C>G , CM000674.2:g.52516720C>G | GRCh38 |
NC_000012.11:g.52910504C>G , CM000674.1:g.52910504C>G | GRCh37 |
NC_000012.10:g.51196771C>G | NCBI36 |
NG_008297.1:g.8740G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252242.9:c.1356G>C MANE Select | ENSP00000252242.4:p.Glu452Asp | |
ENST00000252242.8:c.1356G>C | ENSP00000252242.4:p.Glu452Asp | |
ENST00000547890.5:n.734G>C | ||
ENST00000548409.5:c.478G>C | ||
ENST00000549511.5:n.563G>C | ||
ENST00000552629.5:n.1454G>C | ||
NM_000424.3:c.1356G>C | NP_000415.2:p.Glu452Asp | |
NM_000424.4:c.1356G>C MANE Select | NP_000415.2:p.Glu452Asp |