HGVS | Genome Assembly |
---|---|
NC_000014.9:g.49621831T>A , CM000676.2:g.49621831T>A | GRCh38 |
NC_000014.8:g.50088549T>A , CM000676.1:g.50088549T>A | GRCh37 |
NC_000014.7:g.49158299T>A | NCBI36 |
NG_008920.1:g.6061T>A | |
NG_033054.1:g.3801A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000305386.4:c.563T>A MANE Select | ENSP00000307423.2:p.Phe188Tyr | |
ENST00000305386.3:c.563T>A | ENSP00000307423.2:p.Phe188Tyr | |
NM_002408.3:c.563T>A | NP_002399.1:p.Phe188Tyr | |
NM_002408.4:c.563T>A MANE Select | NP_002399.1:p.Phe188Tyr |