HGVS | Genome Assembly |
---|---|
NC_000015.10:g.64163104T>C , CM000677.2:g.64163104T>C | GRCh38 |
NC_000015.9:g.64455303T>C , CM000677.1:g.64455303T>C | GRCh37 |
NC_000015.8:g.62242356T>C | NCBI36 |
NG_012979.1:g.5052A>G , LRG_10:g.5052A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000680158.1:c.-118A>G | ENSP00000504873.1:n.-118A>G | |
ENST00000300026.3:c.-118A>G | ENSP00000300026.3:n.-118A>G | |
NM_000942.4:c.-118A>G , LRG_10t1:c.-118A>G | NP_000933.1:n.-118A>G |