Canonical Allele Identifier: CA13788922

Genomic Alleles

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

Transcript Alleles

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)