Canonical Allele Identifier: CA2556698014

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.50620336G>A , CM000675.2:g.50620336G>A GRCh38
NC_000013.10:g.51194472G>A , CM000675.1:g.51194472G>A GRCh37
NC_000013.9:g.50092473G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651397.1:n.1033+63570C>T (DLEU7)
ENST00000470726.6:n.347-99311G>A (DLEU1)
ENST00000479420.5:n.560-28254G>A (DLEU1)
ENST00000484869.6:n.1330-10941G>A (DLEU1)