HGVS | Genome Assembly |
---|---|
NC_000015.10:g.48134293T>G , CM000677.2:g.48134293T>G | GRCh38 |
NC_000015.9:g.48426490T>G , CM000677.1:g.48426490T>G | GRCh37 |
NC_000015.8:g.46213782T>G | NCBI36 |
NG_011500.1:g.18322T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000341459.8:c.337T>G MANE Select | ENSP00000341550.3:p.Phe113Val | |
ENST00000341459.7:c.337T>G | ENSP00000341550.3:p.Phe113Val | |
ENST00000449382.2:c.157T>G | ENSP00000389966.2:p.Phe53Val | |
ENST00000463289.1:n.97T>G | ||
NM_205850.2:c.337T>G | NP_995322.1:p.Phe113Val | |
XM_011521458.1:c.337T>G | XP_011519760.1:p.Phe113Val | |
XM_017022079.1:c.-3T>G | XP_016877568.1:n.-3T>G | |
XM_017022080.1:c.-3T>G | XP_016877569.1:n.-3T>G | |
XM_024449901.1:c.-3T>G | XP_024305669.1:n.-3T>G | |
NM_205850.3:c.337T>G MANE Select | NP_995322.1:p.Phe113Val |