HGVS | Genome Assembly |
---|---|
NC_000001.11:g.229432165C= , CM000663.2:g.229432165C= | GRCh38 |
NC_000001.10:g.229567912C= , CM000663.1:g.229567912C= | GRCh37 |
NC_000001.9:g.227634535C= | NCBI36 |
NG_006672.1:g.6932G= , LRG_429:g.6932G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000366683.4:c.637G= | ENSP00000355644.4:p.Asp213= | |
ENST00000684723.1:c.502G= | ENSP00000508084.1:p.Asp168= | |
ENST00000366683.3:c.479+242G= | ENSP00000355644.3:n.479+242G= | |
ENST00000366684.7:c.637G= MANE Select | ENSP00000355645.3:p.Asp213= | |
NM_001100.3:c.637G= , LRG_429t1:c.637G= | NP_001091.1:p.Asp213= | |
NM_001100.4:c.637G= MANE Select | NP_001091.1:p.Asp213= |