HGVS | Genome Assembly |
---|---|
NC_000010.11:g.70441619G>C , CM000672.2:g.70441619G>C | GRCh38 |
NC_000010.10:g.72201375G>C , CM000672.1:g.72201375G>C | GRCh37 |
NC_000010.9:g.71871381G>C | NCBI36 |
NG_012448.1:g.5091C>G | |
NG_012448.2:g.11330C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000287139.8:c.49C>G MANE Select | ENSP00000287139.3:p.Leu17Val | |
ENST00000287139.7:c.49C>G | ENSP00000287139.3:p.Leu17Val | |
ENST00000414871.1:c.29-5636C>G | ENSP00000394468.1:n.29-5636C>G | |
NM_018055.4:c.49C>G | NP_060525.3:p.Leu17Val | |
NM_001329906.1:c.-206-5636C>G | NP_001316835.1:n.-206-5636C>G | |
XM_024448028.1:c.-207+412C>G | XP_024303796.1:n.-207+412C>G | |
NM_018055.5:c.49C>G MANE Select | NP_060525.3:p.Leu17Val | |
NM_001329906.2:c.-206-5636C>G | NP_001316835.1:n.-206-5636C>G |