HGVS | Genome Assembly |
---|---|
NC_000020.11:g.37137934A= , CM000682.2:g.37137934A= | GRCh38 |
NC_000020.10:g.35766337A= , CM000682.1:g.35766337A= | GRCh37 |
NC_000020.9:g.35199751A= | NCBI36 |
NG_033795.1:g.46684T= | |
NG_033795.2:g.46644T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000343811.10:c.1525T= | ENSP00000513568.1:p.Ser509= | |
ENST00000400440.7:c.1525T= | ENSP00000513569.1:p.Ser509= | |
ENST00000421643.2:c.1420T= | ENSP00000513570.1:p.Ser474= | |
ENST00000422138.2:c.1267T= | ENSP00000400468.2:p.Ser423= | |
ENST00000343811.9:n.1594T= | ||
ENST00000343811.8:c.1605T= | ||
ENST00000400440.6:c.1617T= | ||
ENST00000400441.7:c.1525T= | ENSP00000383291.4:p.Ser509= | |
ENST00000417458.5:c.407T= | ||
ENST00000421643.1:c.1529T= |