Canonical Allele Identifier: CA2090971379

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.50620177C= , CM000675.2:g.50620177C= GRCh38
NC_000013.10:g.51194313C= , CM000675.1:g.51194313C= GRCh37
NC_000013.9:g.50092314C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651397.1:n.1033+63729G= (DLEU7)
ENST00000470726.6:n.347-99470C= (DLEU1)
ENST00000479420.5:n.560-28413C= (DLEU1)
ENST00000484869.6:n.1330-11100C= (DLEU1)