HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94041158T= , CM000663.2:g.94041158T= | GRCh38 |
NC_000001.10:g.94506714T= , CM000663.1:g.94506714T= | GRCh37 |
NC_000001.9:g.94279302T= | NCBI36 |
NG_009073.1:g.84992A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.3522+51A= MANE Select | ENSP00000359245.3:n.3522+51A= | |
ENST00000370225.3:c.3522+51A= | ENSP00000359245.3:n.3522+51A= | |
ENST00000536513.5:c.-64-1069A= | ENSP00000439707.2:n.-64-1069A= | |
NM_000350.2:c.3522+51A= | NP_000341.2:n.3522+51A= | |
NM_000350.3:c.3522+51A= MANE Select | NP_000341.2:n.3522+51A= |