HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55154115A= , CM000681.2:g.55154115A= | GRCh38 |
NC_000019.9:g.55665483A= , CM000681.1:g.55665483A= | GRCh37 |
NC_000019.8:g.60357295A= | NCBI36 |
NG_007866.2:g.8618T= , LRG_432:g.8618T= | |
NG_011829.2:g.124T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344887.10:c.464T= MANE Select | ENSP00000341838.5:p.Met155= | |
ENST00000665070.1:c.497T= | ENSP00000499482.1:p.Met166= | |
ENST00000344887.9:c.464T= | ENSP00000341838.5:p.Met155= | |
ENST00000585806.5:n.463T= | ||
ENST00000586669.5:n.472T= | ||
ENST00000588882.1:c.389T= | ENSP00000466729.1:p.Met130= | |
ENST00000589864.1:n.292T= | ||
NM_000363.4:c.464T= , LRG_432t1:c.464T= | NP_000354.4:p.Met155= | |
NM_000363.5:c.464T= MANE Select | NP_000354.4:p.Met155= |