HGVS | Genome Assembly |
---|---|
NC_000021.9:g.46001275C>T , CM000683.2:g.46001275C>T | GRCh38 |
NC_000021.8:g.47421189C>T , CM000683.1:g.47421189C>T | GRCh37 |
NC_000021.7:g.46245617C>T | NCBI36 |
NG_008674.1:g.24527C>T , LRG_475:g.24527C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000463060.6:n.244C>T | ||
ENST00000361866.8:c.1845C>T MANE Select | ENSP00000355180.3:p.Asp615= | |
ENST00000361866.7:c.1845C>T | ENSP00000355180.3:p.Asp615= | |
ENST00000463060.5:n.244C>T | ||
ENST00000498614.5:n.79C>T | ||
ENST00000612273.1:c.1839C>T | ENSP00000483630.1:p.Asp613= | |
NM_001848.2:c.1845C>T , LRG_475t1:c.1845C>T | NP_001839.2:p.Asp615= | |
NM_001848.3:c.1845C>T MANE Select | NP_001839.2:p.Asp615= |