HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52516747C= , CM000674.2:g.52516747C= | GRCh38 |
NC_000012.11:g.52910531C= , CM000674.1:g.52910531C= | GRCh37 |
NC_000012.10:g.51196798C= | NCBI36 |
NG_008297.1:g.8713G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252242.9:c.1329G= MANE Select | ENSP00000252242.4:p.Lys443= | |
ENST00000252242.8:c.1329G= | ENSP00000252242.4:p.Lys443= | |
ENST00000547890.5:n.707G= | ||
ENST00000548409.5:c.451G= | ||
ENST00000549511.5:n.536G= | ||
ENST00000552629.5:n.1427G= | ||
NM_000424.3:c.1329G= | NP_000415.2:p.Lys443= | |
NM_000424.4:c.1329G= MANE Select | NP_000415.2:p.Lys443= |