HGVS | Genome Assembly |
---|---|
NC_000001.11:g.229432288A= , CM000663.2:g.229432288A= | GRCh38 |
NC_000001.10:g.229568035A= , CM000663.1:g.229568035A= | GRCh37 |
NC_000001.9:g.227634658A= | NCBI36 |
NG_006672.1:g.6809T= , LRG_429:g.6809T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000366683.4:c.598T= | ENSP00000355644.4:p.Tyr200= | |
ENST00000684723.1:c.463T= | ENSP00000508084.1:p.Tyr155= | |
ENST00000366683.3:c.479+119T= | ENSP00000355644.3:n.479+119T= | |
ENST00000366684.7:c.598T= MANE Select | ENSP00000355645.3:p.Tyr200= | |
NM_001100.3:c.598T= , LRG_429t1:c.598T= | NP_001091.1:p.Tyr200= | |
NM_001100.4:c.598T= MANE Select | NP_001091.1:p.Tyr200= |