Canonical Allele Identifier: CA185874450
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1002794422
MyVariant Identifiers: chr8:g.129544012C>T (hg19) chr8:g.128531766C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128531766C>T , CM000670.2:g.128531766C>T GRCh38
NC_000008.10:g.129544012C>T , CM000670.1:g.129544012C>T GRCh37
NC_000008.9:g.129613194C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+29304G>A
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