HGVS | Genome Assembly |
---|---|
NC_000013.11:g.50620219C>T , CM000675.2:g.50620219C>T | GRCh38 |
NC_000013.10:g.51194355C>T , CM000675.1:g.51194355C>T | GRCh37 |
NC_000013.9:g.50092356C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000651397.1:n.1033+63687G>A (DLEU7) | ||
ENST00000470726.6:n.347-99428C>T (DLEU1) | ||
ENST00000479420.5:n.560-28371C>T (DLEU1) | ||
ENST00000484869.6:n.1330-11058C>T (DLEU1) |