HGVS | Genome Assembly |
---|---|
NC_000014.9:g.24261837C= , CM000676.2:g.24261837C= | GRCh38 |
NC_000014.8:g.24731043C= , CM000676.1:g.24731043C= | GRCh37 |
NC_000014.7:g.23800883C= | NCBI36 |
NG_007150.1:g.6330G= | |
NG_007150.2:g.6330G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000206765.11:c.366G= MANE Select | ENSP00000206765.6:p.Ser122= | |
ENST00000206765.10:c.366G= | ENSP00000206765.6:p.Ser122= | |
ENST00000544573.5:c.-29+290G= | ENSP00000439446.1:n.-29+290G= | |
ENST00000558074.1:c.366G= | ENSP00000453840.1:p.Ser122= | |
NM_000359.2:c.366G= | NP_000350.1:p.Ser122= | |
NM_000359.3:c.366G= MANE Select | NP_000350.1:p.Ser122= |