HGVS | Genome Assembly |
---|---|
NC_000013.11:g.50542765G>T , CM000675.2:g.50542765G>T | GRCh38 |
NC_000013.10:g.51116901G>T , CM000675.1:g.51116901G>T | GRCh37 |
NC_000013.9:g.50014902G>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000651397.1:n.1034-16758C>A (DLEU7) | ||
ENST00000470726.6:n.346+109215G>T (DLEU1) | ||
ENST00000479420.5:n.458-46710G>T (DLEU1) | ||
ENST00000484869.6:n.1329+39885G>T (DLEU1) |