HGVS | Genome Assembly |
---|---|
NC_000001.11:g.77092285C= , CM000663.2:g.77092285C= | GRCh38 |
NC_000001.10:g.77557970C= , CM000663.1:g.77557970C= | GRCh37 |
NC_000001.9:g.77330558C= | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000370812.8:c.*89G= MANE Select | ENSP00000359848.3:n.*89G= | |
ENST00000370812.7:c.*89G= | ENSP00000359848.3:n.*89G= | |
ENST00000445065.5:c.*89G= | ENSP00000388854.1:n.*89G= | |
ENST00000487906.5:c.850G= | ENSP00000474518.1:n.850G= | |
NM_005482.2:c.*89G= | NP_005473.1:n.*89G= | |
NM_005482.3:c.*89G= MANE Select | NP_005473.1:n.*89G= |