Canonical Allele Identifier: CA249964165

Linked Data

dbSNP Id: rs879479662

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.50620192A>G , CM000675.2:g.50620192A>G GRCh38
NC_000013.10:g.51194328A>G , CM000675.1:g.51194328A>G GRCh37
NC_000013.9:g.50092329A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651397.1:n.1033+63714T>C (DLEU7)
ENST00000470726.6:n.347-99455A>G (DLEU1)
ENST00000479420.5:n.560-28398A>G (DLEU1)
ENST00000484869.6:n.1330-11085A>G (DLEU1)