HGVS | Genome Assembly |
---|---|
NC_000001.11:g.2792641T= , CM000663.2:g.2792641T= | GRCh38 |
NC_000001.10:g.2709206T= , CM000663.1:g.2709206T= | GRCh37 |
NC_000001.9:g.2699066T= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000401095.9:c.785-2295A= MANE Select | ENSP00000383873.4:n.785-2295A= | |
ENST00000401095.8:c.785-2295A= | ENSP00000383873.4:n.785-2295A= | |
NM_001242672.2:c.785-2295A= | NP_001229601.2:n.785-2295A= | |
NM_001242672.3:c.785-2295A= MANE Select | NP_001229601.2:n.785-2295A= |