HGVS | Genome Assembly |
---|---|
NC_000007.14:g.107710089T>G , CM000669.2:g.107710089T>G | GRCh38 |
NC_000007.13:g.107350534T>G , CM000669.1:g.107350534T>G | GRCh37 |
NC_000007.12:g.107137770T>G | NCBI36 |
NG_008489.1:g.54455T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000644269.2:c.2125T>G MANE Select | ENSP00000494017.1:p.Phe709Val | |
ENST00000644846.1:c.781T>G | ||
ENST00000265715.7:c.2125T>G | ENSP00000265715.3:p.Phe709Val | |
ENST00000492030.2:n.377-66T>G | ||
NM_000441.1:c.2125T>G | NP_000432.1:p.Phe709Val | |
XM_005250425.1:c.2125T>G | XP_005250482.1:p.Phe709Val | |
XM_005250425.2:c.2125T>G | XP_005250482.1:p.Phe709Val | |
XM_017012318.1:c.2047T>G | XP_016867807.1:p.Phe683Val | |
NM_000441.2:c.2125T>G MANE Select | NP_000432.1:p.Phe709Val |