HGVS | Genome Assembly |
---|---|
NC_000001.11:g.40838389C>A , CM000663.2:g.40838389C>A | GRCh38 |
NC_000001.10:g.41304061C>A , CM000663.1:g.41304061C>A | GRCh37 |
NC_000001.9:g.41076648C>A | NCBI36 |
NG_008139.1:g.59378C>A | |
NG_008139.2:g.59378C>A | |
NG_008139.3:g.59603C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000347132.10:c.1954C>A MANE Select | ENSP00000262916.6:p.Leu652Met | |
ENST00000347132.9:c.1954C>A | ENSP00000262916.6:p.Leu652Met | |
ENST00000443478.3:c.1535C>A | ||
ENST00000506017.1:n.1273C>A | ||
ENST00000509682.6:c.1792C>A | ENSP00000423756.2:p.Leu598Met | |
NM_004700.3:c.1954C>A | NP_004691.2:p.Leu652Met | |
NM_172163.2:c.1792C>A | NP_751895.1:p.Leu598Met | |
XM_017002792.1:c.937C>A | XP_016858281.1:p.Leu313Met | |
NM_004700.4:c.1954C>A MANE Select | NP_004691.2:p.Leu652Met | |
NM_172163.3:c.1792C>A | NP_751895.1:p.Leu598Met |