Canonical Allele Identifier: CA698828754

Linked Data

dbSNP Id: rs1474968710

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.50620226C>T , CM000675.2:g.50620226C>T GRCh38
NC_000013.10:g.51194362C>T , CM000675.1:g.51194362C>T GRCh37
NC_000013.9:g.50092363C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651397.1:n.1033+63680G>A (DLEU7)
ENST00000470726.6:n.347-99421C>T (DLEU1)
ENST00000479420.5:n.560-28364C>T (DLEU1)
ENST00000484869.6:n.1330-11051C>T (DLEU1)