HGVS | Genome Assembly |
---|---|
NC_000001.11:g.229432756T= , CM000663.2:g.229432756T= | GRCh38 |
NC_000001.10:g.229568503T= , CM000663.1:g.229568503T= | GRCh37 |
NC_000001.9:g.227635126T= | NCBI36 |
NG_006672.1:g.6341A= , LRG_429:g.6341A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000366683.4:c.254A= | ENSP00000355644.4:p.Glu85= | |
ENST00000684723.1:c.119A= | ENSP00000508084.1:p.Glu40= | |
ENST00000366683.3:c.254A= | ENSP00000355644.3:p.Glu85= | |
ENST00000366684.7:c.254A= MANE Select | ENSP00000355645.3:p.Glu85= | |
NM_001100.3:c.254A= , LRG_429t1:c.254A= | NP_001091.1:p.Glu85= | |
NM_001100.4:c.254A= MANE Select | NP_001091.1:p.Glu85= |