Canonical Allele Identifier: CA1818917130
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs567745951
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128554857G>A , CM000670.2:g.128554857G>A GRCh38
NC_000008.10:g.129567103G>A , CM000670.1:g.129567103G>A GRCh37
NC_000008.9:g.129636285G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121672.1:n.508+6213C>T
Search 100 bp 5'
Search 100 bp 3'