HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154187842T>A , CM000685.2:g.154187842T>A | GRCh38 |
NC_000023.10:g.153453331T>A , CM000685.1:g.153453331T>A | GRCh37 |
NG_011606.1:g.10247T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000595290.6:c.185T>A MANE Select | ENSP00000472316.1:p.Phe62Tyr | |
ENST00000595290.5:c.185T>A | ENSP00000472316.1:p.Phe62Tyr | |
ENST00000595330.1:n.195T>A | ||
NM_000513.2:c.185T>A MANE Select | NP_000504.1:p.Phe62Tyr |