HGVS | Genome Assembly |
---|---|
NC_000014.9:g.24256045A>T , CM000676.2:g.24256045A>T | GRCh38 |
NC_000014.8:g.24725251A>T , CM000676.1:g.24725251A>T | GRCh37 |
NC_000014.7:g.23795091A>T | NCBI36 |
NG_007150.1:g.12122T>A | |
NG_007150.2:g.12122T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000206765.11:c.1435T>A MANE Select | ENSP00000206765.6:p.Ser479Thr | |
ENST00000206765.10:c.1435T>A | ENSP00000206765.6:p.Ser479Thr | |
ENST00000544573.5:c.109T>A | ENSP00000439446.1:p.Ser37Thr | |
ENST00000559136.1:c.508T>A | ENSP00000453337.1:p.Ser170Thr | |
NM_000359.2:c.1435T>A | NP_000350.1:p.Ser479Thr | |
NM_000359.3:c.1435T>A MANE Select | NP_000350.1:p.Ser479Thr |