Canonical Allele Identifier: CA2018069081

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.50537219T= , CM000675.2:g.50537219T= GRCh38
NC_000013.10:g.51111355T= , CM000675.1:g.51111355T= GRCh37
NC_000013.9:g.50009356T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651397.1:n.1034-11212A= (DLEU7)
ENST00000470726.6:n.346+103669T= (DLEU1)
ENST00000479420.5:n.457+44458T= (DLEU1)
ENST00000484869.6:n.1329+34339T= (DLEU1)