Canonical Allele Identifier: CA698828784
Gene: DLEU7 HGNC NCBI
DLEU1 HGNC NCBI

Linked Data

dbSNP Id: rs1259672497
MyVariant Identifiers: chr13:g.51194414A>T (hg19) chr13:g.50620278A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.50620278A>T , CM000675.2:g.50620278A>T GRCh38
NC_000013.10:g.51194414A>T , CM000675.1:g.51194414A>T GRCh37
NC_000013.9:g.50092415A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651397.1:n.1033+63628T>A (DLEU7)
ENST00000470726.6:n.347-99369A>T (DLEU1)
ENST00000479420.5:n.560-28312A>T (DLEU1)
ENST00000484869.6:n.1330-10999A>T (DLEU1)
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