HGVS | Genome Assembly |
---|---|
NC_000016.10:g.86510660T>A , CM000678.2:g.86510660T>A | GRCh38 |
NC_000016.9:g.86544266T>A , CM000678.1:g.86544266T>A | GRCh37 |
NC_000016.8:g.85101767T>A | NCBI36 |
NG_016273.1:g.5134T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262426.6:c.91T>A MANE Select | ENSP00000262426.4:p.Ser31Thr | |
ENST00000262426.5:c.91T>A | ENSP00000262426.4:p.Ser31Thr | |
NM_001451.2:c.91T>A | NP_001442.2:p.Ser31Thr | |
NM_001451.3:c.91T>A MANE Select | NP_001442.2:p.Ser31Thr |