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