HGVS | Genome Assembly |
---|---|
NC_000014.9:g.24258896C= , CM000676.2:g.24258896C= | GRCh38 |
NC_000014.8:g.24728102C= , CM000676.1:g.24728102C= | GRCh37 |
NC_000014.7:g.23797942C= | NCBI36 |
NG_007150.1:g.9271G= | |
NG_007150.2:g.9271G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000206765.11:c.1159+179G= MANE Select | ENSP00000206765.6:n.1159+179G= | |
ENST00000206765.10:c.1159+179G= | ENSP00000206765.6:n.1159+179G= | |
ENST00000544573.5:c.-28-508G= | ENSP00000439446.1:n.-28-508G= | |
ENST00000559136.1:c.232+179G= | ENSP00000453337.1:n.232+179G= | |
NM_000359.2:c.1159+179G= | NP_000350.1:n.1159+179G= | |
NM_000359.3:c.1159+179G= MANE Select | NP_000350.1:n.1159+179G= |