Canonical Allele Identifier: CA2090971429

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.50620286T= , CM000675.2:g.50620286T= GRCh38
NC_000013.10:g.51194422T= , CM000675.1:g.51194422T= GRCh37
NC_000013.9:g.50092423T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651397.1:n.1033+63620A= (DLEU7)
ENST00000470726.6:n.347-99361T= (DLEU1)
ENST00000479420.5:n.560-28304T= (DLEU1)
ENST00000484869.6:n.1330-10991T= (DLEU1)