Canonical Allele Identifier: CA1119097464
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs941001567
gnomAD v3: 8-128529870-C-A
gnomAD v4: 8-128529870-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128529870C>A , CM000670.2:g.128529870C>A GRCh38
NC_000008.10:g.129542116C>A , CM000670.1:g.129542116C>A GRCh37
NC_000008.9:g.129611298C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+31200G>T
Search 100 bp 5'
Search 100 bp 3'