HGVS | Genome Assembly |
---|---|
NC_000021.9:g.44456699T>A , CM000683.2:g.44456699T>A | GRCh38 |
NC_000021.8:g.45876582T>A , CM000683.1:g.45876582T>A | GRCh37 |
NC_000021.7:g.44701010T>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000291592.6:c.55T>A MANE Select | ENSP00000291592.4:p.Ser19Thr | |
ENST00000291592.5:c.55T>A | ENSP00000291592.4:p.Ser19Thr | |
NM_030891.4:c.55T>A | NP_112153.1:p.Ser19Thr | |
NM_030891.5:c.55T>A | NP_112153.1:p.Ser19Thr | |
NM_030891.6:c.55T>A MANE Select | NP_112153.1:p.Ser19Thr |