HGVS | Genome Assembly |
---|---|
NC_000020.11:g.57565373T>G , CM000682.2:g.57565373T>G | GRCh38 |
NC_000020.10:g.56140429T>G , CM000682.1:g.56140429T>G | GRCh37 |
NC_000020.9:g.55573835T>G | NCBI36 |
NG_008205.1:g.9293T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000319441.6:c.1438T>G MANE Select | ENSP00000319814.4:p.Phe480Val | |
ENST00000319441.5:c.1438T>G | ENSP00000319814.4:p.Phe480Val | |
ENST00000467047.1:n.4080T>G | ||
ENST00000485958.1:n.562T>G | ||
NM_002591.3:c.1438T>G | NP_002582.3:p.Phe480Val | |
XM_011528839.1:c.1042T>G | XP_011527141.1:p.Phe348Val | |
XM_024451888.1:c.1042T>G | XP_024307656.1:p.Phe348Val | |
NM_002591.4:c.1438T>G MANE Select | NP_002582.3:p.Phe480Val |