HGVS | Genome Assembly |
---|---|
NC_000019.10:g.10115575A>T , CM000681.2:g.10115575A>T | GRCh38 |
NC_000019.9:g.10226251A>T , CM000681.1:g.10226251A>T | GRCh37 |
NC_000019.8:g.10087251A>T | NCBI36 |
NG_047007.1:g.9055A>T | |
NG_051197.1:g.9350T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000253108.9:c.851T>A MANE Select | ENSP00000253108.3:p.Phe284Tyr | |
ENST00000253108.8:c.851T>A | ENSP00000253108.3:p.Phe284Tyr | |
ENST00000589454.5:c.827T>A | ENSP00000466860.1:p.Phe276Tyr | |
ENST00000590158.1:n.870T>A | ||
ENST00000593054.5:c.245T>A | ENSP00000467187.1:p.Phe82Tyr | |
NM_003755.3:c.851T>A | NP_003746.2:p.Phe284Tyr | |
NM_003755.4:c.851T>A | NP_003746.2:p.Phe284Tyr | |
NM_003755.5:c.851T>A MANE Select | NP_003746.2:p.Phe284Tyr |