Canonical Allele Identifier: CA698828793
Gene: DLEU7 HGNC NCBI
DLEU1 HGNC NCBI

Linked Data

dbSNP Id: rs1229716578
gnomAD v3: 13-50620302-A-G
gnomAD v4: 13-50620302-A-G
MyVariant Identifiers: chr13:g.51194438A>G (hg19) chr13:g.50620302A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.50620302A>G , CM000675.2:g.50620302A>G GRCh38
NC_000013.10:g.51194438A>G , CM000675.1:g.51194438A>G GRCh37
NC_000013.9:g.50092439A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651397.1:n.1033+63604T>C (DLEU7)
ENST00000470726.6:n.347-99345A>G (DLEU1)
ENST00000479420.5:n.560-28288A>G (DLEU1)
ENST00000484869.6:n.1330-10975A>G (DLEU1)
Search 100 bp 5'
Search 100 bp 3'