HGVS | Genome Assembly |
---|---|
NC_000002.12:g.218782746G= , CM000664.2:g.218782746G= | GRCh38 |
NC_000002.11:g.219647469G= , CM000664.1:g.219647469G= | GRCh37 |
NC_000002.10:g.219355713G= | NCBI36 |
NG_007959.1:g.5998G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000258415.9:c.255+309G= MANE Select | ENSP00000258415.4:n.255+309G= | |
ENST00000258415.8:c.255+309G= | ENSP00000258415.4:n.255+309G= | |
ENST00000445971.1:c.255+309G= | ENSP00000404945.1:n.255+309G= | |
ENST00000466602.1:n.264+309G= | ||
ENST00000494263.5:n.689+309G= | ||
NM_000784.3:c.255+309G= | NP_000775.1:n.255+309G= | |
XM_017003488.2:c.26+309G= | XP_016858977.1:n.26+309G= | |
NM_000784.4:c.255+309G= MANE Select | NP_000775.1:n.255+309G= |