HGVS | Genome Assembly |
---|---|
NC_000019.10:g.51746313T= , CM000681.2:g.51746313T= | GRCh38 |
NC_000019.9:g.52249566T= , CM000681.1:g.52249566T= | GRCh37 |
NC_000019.8:g.56941378T= | NCBI36 |
NG_023426.1:g.10585A= , LRG_146:g.10585A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000594900.2:c.682A= | ENSP00000470750.2:p.Ile228= | |
ENST00000600815.2:c.682A= | ENSP00000472936.2:p.Ile228= | |
ENST00000304748.5:c.682A= MANE Select | ENSP00000302707.3:p.Ile228= | |
ENST00000304748.4:c.682A= | ENSP00000302707.3:p.Ile228= | |
ENST00000595042.5:c.682A= | ENSP00000471493.1:p.Ile228= | |
NM_001193306.1:c.682A= | NP_001180235.1:p.Ile228= | |
NM_002029.3:c.682A= , LRG_146t1:c.682A= | NP_002020.1:p.Ile228= | |
NM_001193306.2:c.682A= | NP_001180235.1:p.Ile228= | |
NM_002029.4:c.682A= MANE Select | NP_002020.1:p.Ile228= |