HGVS | Genome Assembly |
---|---|
NC_000014.9:g.100883203T= , CM000676.2:g.100883203T= | GRCh38 |
NC_000014.8:g.101349540T= , CM000676.1:g.101349540T= | GRCh37 |
NC_000014.7:g.100419293T= | NCBI36 |
NG_045001.1:g.6645A= | |
NG_045000.5:g.51935T= | |
NG_045000.6:g.51935T= | |
NG_045001.2:g.25520A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000649591.1:c.1586A= MANE Select | ENSP00000497482.1:p.Tyr529= | |
ENST00000534062.1:c.1586A= | ENSP00000435342.1:p.Tyr529= | |
NM_001134888.2:c.1586A= | NP_001128360.1:p.Tyr529= | |
NM_001134888.3:c.1586A= MANE Select | NP_001128360.1:p.Tyr529= |