Canonical Allele Identifier: CA185876392
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs957656612
MyVariant Identifiers: chr8:g.129559459C>A (hg19) chr8:g.128547213C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128547213C>A , CM000670.2:g.128547213C>A GRCh38
NC_000008.10:g.129559459C>A , CM000670.1:g.129559459C>A GRCh37
NC_000008.9:g.129628641C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+13857G>T
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