HGVS | Genome Assembly |
---|---|
NC_000013.11:g.50620235A>G , CM000675.2:g.50620235A>G | GRCh38 |
NC_000013.10:g.51194371A>G , CM000675.1:g.51194371A>G | GRCh37 |
NC_000013.9:g.50092372A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000651397.1:n.1033+63671T>C (DLEU7) | ||
ENST00000470726.6:n.347-99412A>G (DLEU1) | ||
ENST00000479420.5:n.560-28355A>G (DLEU1) | ||
ENST00000484869.6:n.1330-11042A>G (DLEU1) |