HGVS | Genome Assembly |
---|---|
NC_000003.12:g.28662972A>G , CM000665.2:g.28662972A>G | GRCh38 |
NC_000003.11:g.28704463A>G , CM000665.1:g.28704463A>G | GRCh37 |
NC_000003.10:g.28679467A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000432518.6:n.809+86476A>G | ||
ENST00000443912.5:n.87-73037A>G | ||
ENST00000445077.1:n.69+86476A>G | ||
ENST00000635992.1:c.*339+86476A>G | ENSP00000489994.1:n.*339+86476A>G | |
ENST00000636680.2:c.213+86476A>G (RBMS3) | ENSP00000490271.2:n.213+86476A>G | |
NR_038840.1:n.322+86476A>G (LINC00693) |