HGVS | Genome Assembly |
---|---|
NC_000004.12:g.4862889T>G , CM000666.2:g.4862889T>G | GRCh38 |
NC_000004.11:g.4864616T>G , CM000666.1:g.4864616T>G | GRCh37 |
NC_000004.10:g.4915517T>G | NCBI36 |
NG_008121.1:g.8225T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382723.5:c.658T>G MANE Select | ENSP00000372170.4:p.Phe220Val | |
ENST00000382723.4:c.658T>G | ENSP00000372170.4:p.Phe220Val | |
ENST00000468421.1:n.370T>G | ||
NM_002448.3:c.658T>G MANE Select | NP_002439.2:p.Phe220Val |