Canonical Allele Identifier: CA185874430
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs912848622
MyVariant Identifiers: chr8:g.128531659G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128531659G>C , CM000670.2:g.128531659G>C GRCh38
NC_000008.10:g.129543905G>C , CM000670.1:g.129543905G>C GRCh37
NC_000008.9:g.129613087G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121672.1:n.508+29411C>G
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