HGVS | Genome Assembly |
---|---|
NC_000020.11:g.46011187T= , CM000682.2:g.46011187T= | GRCh38 |
NC_000020.10:g.44639826T= , CM000682.1:g.44639826T= | GRCh37 |
NC_000020.9:g.44073233T= | NCBI36 |
NG_011468.1:g.7280T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372330.3:c.694T= MANE Select | ENSP00000361405.3:p.Phe232= | |
NM_004994.2:c.694T= | NP_004985.2:p.Phe232= | |
NM_004994.3:c.694T= MANE Select | NP_004985.2:p.Phe232= |