HGVS | Genome Assembly |
---|---|
NC_000013.11:g.50620199T>C , CM000675.2:g.50620199T>C | GRCh38 |
NC_000013.10:g.51194335T>C , CM000675.1:g.51194335T>C | GRCh37 |
NC_000013.9:g.50092336T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000651397.1:n.1033+63707A>G (DLEU7) | ||
ENST00000470726.6:n.347-99448T>C (DLEU1) | ||
ENST00000479420.5:n.560-28391T>C (DLEU1) | ||
ENST00000484869.6:n.1330-11078T>C (DLEU1) |