Canonical Allele Identifier: CA13895660

Gene: DLEU7 DLEU1

Linked Data

• dbSNP Id: rs192322009
• gnomAD v2: 13-51194318-C-T
• gnomAD v3: 13-50620182-C-T
• gnomAD v4: 13-50620182-C-T
• MyVariant Identifiers: chr13:g.51194318C>T (hg19) ; chr13:g.50620182C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.50620182C>T , CM000675.2:g.50620182C>T	GRCh38
NC_000013.10:g.51194318C>T , CM000675.1:g.51194318C>T	GRCh37
NC_000013.9:g.50092319C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651397.1:n.1033+63724G>A (DLEU7)
ENST00000470726.6:n.347-99465C>T (DLEU1)
ENST00000479420.5:n.560-28408C>T (DLEU1)
ENST00000484869.6:n.1330-11095C>T (DLEU1)