Canonical Allele Identifier: CA955960115

Linked Data

dbSNP Id: rs1871535027

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.50620277C>T , CM000675.2:g.50620277C>T GRCh38
NC_000013.10:g.51194413C>T , CM000675.1:g.51194413C>T GRCh37
NC_000013.9:g.50092414C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651397.1:n.1033+63629G>A (DLEU7)
ENST00000470726.6:n.347-99370C>T (DLEU1)
ENST00000479420.5:n.560-28313C>T (DLEU1)
ENST00000484869.6:n.1330-11000C>T (DLEU1)