Canonical Allele Identifier: CA2090971420

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.50620275T= , CM000675.2:g.50620275T= GRCh38
NC_000013.10:g.51194411T= , CM000675.1:g.51194411T= GRCh37
NC_000013.9:g.50092412T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651397.1:n.1033+63631A= (DLEU7)
ENST00000470726.6:n.347-99372T= (DLEU1)
ENST00000479420.5:n.560-28315T= (DLEU1)
ENST00000484869.6:n.1330-11002T= (DLEU1)