Canonical Allele Identifier: CA2090971424

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.50620280C= , CM000675.2:g.50620280C= GRCh38
NC_000013.10:g.51194416C= , CM000675.1:g.51194416C= GRCh37
NC_000013.9:g.50092417C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651397.1:n.1033+63626G= (DLEU7)
ENST00000470726.6:n.347-99367C= (DLEU1)
ENST00000479420.5:n.560-28310C= (DLEU1)
ENST00000484869.6:n.1330-10997C= (DLEU1)