HGVS | Genome Assembly |
---|---|
NC_000011.10:g.121307381C>A , CM000673.2:g.121307381C>A | GRCh38 |
NC_000011.9:g.121178090C>A , CM000673.1:g.121178090C>A | GRCh37 |
NC_000011.8:g.120683300C>A | NCBI36 |
NG_009446.1:g.19703C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264027.9:c.769C>A MANE Select | ENSP00000264027.4:p.Pro257Thr | |
ENST00000264027.8:c.769C>A | ENSP00000264027.4:p.Pro257Thr | |
ENST00000392789.2:c.769C>A | ENSP00000376539.2:p.Pro257Thr | |
ENST00000527183.1:n.1062C>A | ||
ENST00000534230.5:c.632-76C>A | ENSP00000432550.1:n.632-76C>A | |
NM_001024956.2:c.769C>A | NP_001020127.1:p.Pro257Thr | |
NM_006918.4:c.769C>A | NP_008849.2:p.Pro257Thr | |
NM_006918.5:c.769C>A MANE Select | NP_008849.2:p.Pro257Thr | |
NM_001024956.3:c.769C>A | NP_001020127.1:p.Pro257Thr |