HGVS | Genome Assembly |
---|---|
NC_000019.10:g.45766979A>T , CM000681.2:g.45766979A>T | GRCh38 |
NC_000019.9:g.46270237A>T , CM000681.1:g.46270237A>T | GRCh37 |
NC_000019.8:g.50962077A>T | NCBI36 |
NG_012745.1:g.7261T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000317578.7:c.980T>A MANE Select | ENSP00000316842.4:p.Phe327Tyr | |
ENST00000317578.6:c.980T>A | ENSP00000316842.4:p.Phe327Tyr | |
ENST00000560160.1:c.587-868T>A | ||
ENST00000560168.1:c.*168T>A | ENSP00000453189.2:n.*168T>A | |
ENST00000622857.1:c.16-1017T>A | ENSP00000481365.1:n.16-1017T>A | |
NM_175875.4:c.980T>A | NP_787071.2:p.Phe327Tyr | |
NM_175875.5:c.980T>A MANE Select | NP_787071.3:p.Phe327Tyr |