HGVS | Genome Assembly |
---|---|
NC_000021.9:g.45984395C= , CM000683.2:g.45984395C= | GRCh38 |
NC_000021.8:g.47404309C= , CM000683.1:g.47404309C= | GRCh37 |
NC_000021.7:g.46228737C= | NCBI36 |
NG_008674.1:g.7647C= , LRG_475:g.7647C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361866.8:c.354C= MANE Select | ENSP00000355180.3:p.Asp118= | |
ENST00000361866.7:c.354C= | ENSP00000355180.3:p.Asp118= | |
ENST00000612273.1:c.354C= | ENSP00000483630.1:p.Asp118= | |
NM_001848.2:c.354C= , LRG_475t1:c.354C= | NP_001839.2:p.Asp118= | |
NM_001848.3:c.354C= MANE Select | NP_001839.2:p.Asp118= |