Canonical Allele Identifier: CA1818921093
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1816085830
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128529693G>A , CM000670.2:g.128529693G>A GRCh38
NC_000008.10:g.129541939G>A , CM000670.1:g.129541939G>A GRCh37
NC_000008.9:g.129611121G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+31377C>T
Search 100 bp 5'
Search 100 bp 3'