Canonical Allele Identifier: CA185874447
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs906828546
gnomAD v2: 8-129543997-A-G
gnomAD v3: 8-128531751-A-G
gnomAD v4: 8-128531751-A-G
MyVariant Identifiers: chr8:g.129543997A>G (hg19) chr8:g.128531751A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128531751A>G , CM000670.2:g.128531751A>G GRCh38
NC_000008.10:g.129543997A>G , CM000670.1:g.129543997A>G GRCh37
NC_000008.9:g.129613179A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121672.1:n.508+29319T>C
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