HGVS | Genome Assembly |
---|---|
NC_000019.10:g.51746404C= , CM000681.2:g.51746404C= | GRCh38 |
NC_000019.9:g.52249657C= , CM000681.1:g.52249657C= | GRCh37 |
NC_000019.8:g.56941469C= | NCBI36 |
NG_023426.1:g.10494G= , LRG_146:g.10494G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000594900.2:c.591G= | ENSP00000470750.2:p.Met197= | |
ENST00000600815.2:c.591G= | ENSP00000472936.2:p.Met197= | |
ENST00000304748.5:c.591G= MANE Select | ENSP00000302707.3:p.Met197= | |
ENST00000304748.4:c.591G= | ENSP00000302707.3:p.Met197= | |
ENST00000595042.5:c.591G= | ENSP00000471493.1:p.Met197= | |
NM_001193306.1:c.591G= | NP_001180235.1:p.Met197= | |
NM_002029.3:c.591G= , LRG_146t1:c.591G= | NP_002020.1:p.Met197= | |
NM_001193306.2:c.591G= | NP_001180235.1:p.Met197= | |
NM_002029.4:c.591G= MANE Select | NP_002020.1:p.Met197= |