HGVS | Genome Assembly |
---|---|
NC_000011.10:g.124872875C= , CM000673.2:g.124872875C= | GRCh38 |
NC_000011.9:g.124742771C= , CM000673.1:g.124742771C= | GRCh37 |
NC_000011.8:g.124247981C= | NCBI36 |
NG_016214.1:g.12467C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000397801.6:c.1331-9C= MANE Select | ENSP00000380903.1:n.1331-9C= | |
ENST00000397801.5:c.1331-9C= | ENSP00000380903.1:n.1331-9C= | |
ENST00000538940.5:c.1265-9C= | ENSP00000441797.1:n.1265-9C= | |
NM_022370.3:c.1331-9C= | NP_071765.2:n.1331-9C= | |
XM_011542953.1:c.2303-9C= | XP_011541255.1:n.2303-9C= | |
XM_017018122.1:c.1265-9C= | XP_016873611.1:n.1265-9C= | |
NM_022370.4:c.1331-9C= MANE Select | NP_071765.2:n.1331-9C= |