HGVS | Genome Assembly |
---|---|
NC_000002.12:g.218813882G>A , CM000664.2:g.218813882G>A | GRCh38 |
NC_000002.11:g.219678605G>A , CM000664.1:g.219678605G>A | GRCh37 |
NC_000002.10:g.219386849G>A | NCBI36 |
NG_007959.1:g.37134G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000258415.9:c.1018-139G>A MANE Select | ENSP00000258415.4:n.1018-139G>A | |
ENST00000258415.8:c.1018-139G>A | ENSP00000258415.4:n.1018-139G>A | |
ENST00000445971.1:c.*479-139G>A | ENSP00000404945.1:n.*479-139G>A | |
ENST00000466602.1:n.1140-139G>A | ||
ENST00000494263.5:n.1452-139G>A | ||
NM_000784.3:c.1018-139G>A | NP_000775.1:n.1018-139G>A | |
XM_017003488.2:c.598-139G>A | XP_016858977.1:n.598-139G>A | |
NM_000784.4:c.1018-139G>A MANE Select | NP_000775.1:n.1018-139G>A |