Canonical Allele Identifier: CA1818909589
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1563634301
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128547214A>C , CM000670.2:g.128547214A>C GRCh38
NC_000008.10:g.129559460A>C , CM000670.1:g.129559460A>C GRCh37
NC_000008.9:g.129628642A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+13856T>G
Search 100 bp 5'
Search 100 bp 3'