HGVS | Genome Assembly |
---|---|
NC_000002.12:g.68218277C= , CM000664.2:g.68218277C= | GRCh38 |
NC_000002.11:g.68445409C= , CM000664.1:g.68445409C= | GRCh37 |
NC_000002.10:g.68298913C= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000234310.8:c.4-1146G= MANE Select | ENSP00000234310.3:n.4-1146G= | |
ENST00000234310.7:c.4-1146G= | ENSP00000234310.3:n.4-1146G= | |
ENST00000406334.3:c.-27-1146G= | ENSP00000384974.3:n.-27-1146G= | |
ENST00000409377.1:c.-27-1146G= | ENSP00000387148.1:n.-27-1146G= | |
ENST00000409752.5:c.61-1146G= | ENSP00000387216.1:n.61-1146G= | |
NM_000945.3:c.4-1146G= | NP_000936.1:n.4-1146G= | |
NM_000945.4:c.4-1146G= MANE Select | NP_000936.1:n.4-1146G= |