HGVS | Genome Assembly |
---|---|
NC_000001.11:g.119140764A>T , CM000663.2:g.119140764A>T | GRCh38 |
NC_000001.10:g.119683387A>T , CM000663.1:g.119683387A>T | GRCh37 |
NC_000001.9:g.119484910A>T | NCBI36 |
NG_050658.1:g.5025T>A |
HGVS | Amino-acid Change | |
---|---|---|
NR_125974.1:n.369A>T (WARS2-AS1) | ||
NR_125975.1:n.369A>T (WARS2-AS1) | ||
NR_125976.1:n.369A>T (WARS2-AS1) | ||
NR_125977.1:n.369A>T (WARS2-AS1) | ||
XM_006710283.1:c.-689T>A (WARS2) | XP_006710346.1:n.-689T>A | |
XM_011540493.1:c.-561T>A (WARS2) | XP_011538795.1:n.-561T>A | |
XM_011540495.1:c.-120T>A (WARS2) | XP_011538797.1:n.-120T>A | |
XM_017000041.2:c.-689T>A (WARS2) | XP_016855530.1:n.-689T>A | |
XM_024449826.1:c.-561T>A (WARS2) | XP_024305594.1:n.-561T>A | |
XM_024449860.1:c.-689T>A (WARS2) | XP_024305628.1:n.-689T>A |