HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4631863T= , CM000679.2:g.4631863T= | GRCh38 |
NC_000017.10:g.4535158T= , CM000679.1:g.4535158T= | GRCh37 |
NC_000017.9:g.4481907T= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293761.8:c.1809+26A= MANE Select | ENSP00000293761.3:n.1809+26A= | |
ENST00000570836.6:c.1809+26A= | ENSP00000458832.1:n.1809+26A= | |
ENST00000293761.7:c.1809+26A= | ENSP00000293761.3:n.1809+26A= | |
ENST00000570836.5:c.1809+26A= | ENSP00000458832.1:n.1809+26A= | |
ENST00000574640.1:c.1692+26A= | ENSP00000460483.1:n.1692+26A= | |
NM_001140.3:c.1809+26A= | NP_001131.3:n.1809+26A= | |
NM_001140.4:c.1809+26A= | NP_001131.3:n.1809+26A= | |
NM_001140.5:c.1809+26A= MANE Select | NP_001131.3:n.1809+26A= |