HGVS | Genome Assembly |
---|---|
NC_000005.10:g.10286360C>G , CM000667.2:g.10286360C>G | GRCh38 |
NC_000005.9:g.10286472C>G , CM000667.1:g.10286472C>G | GRCh37 |
NC_000005.8:g.10339472C>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000296658.4:c.460G>C MANE Select | ENSP00000296658.3:p.Val154Leu | |
ENST00000296658.3:c.460G>C | ENSP00000296658.3:p.Val154Leu | |
ENST00000506821.1:n.714G>C | ||
ENST00000510532.5:n.528G>C | ||
ENST00000511963.5:n.568G>C | ||
NM_138809.3:c.460G>C | NP_620164.1:p.Val154Leu | |
NM_138809.4:c.460G>C MANE Select | NP_620164.1:p.Val154Leu |