HGVS | Genome Assembly |
---|---|
NC_000002.12:g.218812800G= , CM000664.2:g.218812800G= | GRCh38 |
NC_000002.11:g.219677523G= , CM000664.1:g.219677523G= | GRCh37 |
NC_000002.10:g.219385767G= | NCBI36 |
NG_007959.1:g.36052G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000258415.9:c.844+51G= MANE Select | ENSP00000258415.4:n.844+51G= | |
ENST00000258415.8:c.844+51G= | ENSP00000258415.4:n.844+51G= | |
ENST00000411688.1:c.562+51G= | ENSP00000392671.1:n.562+51G= | |
ENST00000445971.1:c.*305+51G= | ENSP00000404945.1:n.*305+51G= | |
ENST00000466602.1:n.843G= | ||
ENST00000494263.5:n.1278+51G= | ||
NM_000784.3:c.844+51G= | NP_000775.1:n.844+51G= | |
XM_017003488.2:c.424+51G= | XP_016858977.1:n.424+51G= | |
NM_000784.4:c.844+51G= MANE Select | NP_000775.1:n.844+51G= |