HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52516733C>G , CM000674.2:g.52516733C>G | GRCh38 |
NC_000012.11:g.52910517C>G , CM000674.1:g.52910517C>G | GRCh37 |
NC_000012.10:g.51196784C>G | NCBI36 |
NG_008297.1:g.8727G>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000252242.9:c.1343G>C MANE Select | ENSP00000252242.4:p.Arg448Pro | |
ENST00000252242.8:c.1343G>C | ENSP00000252242.4:p.Arg448Pro | |
ENST00000547890.5:n.721G>C | ||
ENST00000548409.5:c.465G>C | ||
ENST00000549511.5:n.550G>C | ||
ENST00000552629.5:n.1441G>C | ||
NM_000424.3:c.1343G>C | NP_000415.2:p.Arg448Pro | |
NM_000424.4:c.1343G>C MANE Select | NP_000415.2:p.Arg448Pro |