HGVS | Genome Assembly |
---|---|
NC_000023.11:g.50916269T>A , CM000685.2:g.50916269T>A | GRCh38 |
NC_000023.10:g.50659269T>A , CM000685.1:g.50659269T>A | GRCh37 |
NC_000023.9:g.50676009T>A | NCBI36 |
NG_012894.1:g.10486T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252677.4:c.841T>A MANE Select | ENSP00000252677.3:p.Ser281Thr | |
ENST00000252677.3:c.841T>A | ENSP00000252677.3:p.Ser281Thr | |
NM_005448.2:c.841T>A MANE Select | NP_005439.2:p.Ser281Thr |