Canonical Allele Identifier: CA2090971458

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.50620365A= , CM000675.2:g.50620365A= GRCh38
NC_000013.10:g.51194501A= , CM000675.1:g.51194501A= GRCh37
NC_000013.9:g.50092502A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651397.1:n.1033+63541T= (DLEU7)
ENST00000470726.6:n.347-99282A= (DLEU1)
ENST00000479420.5:n.560-28225A= (DLEU1)
ENST00000484869.6:n.1330-10912A= (DLEU1)