Canonical Allele Identifier: CA185874171
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs574708611
gnomAD v3: 8-128529895-A-G
gnomAD v4: 8-128529895-A-G
MyVariant Identifiers: chr8:g.129542141A>G (hg19) chr8:g.128529895A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128529895A>G , CM000670.2:g.128529895A>G GRCh38
NC_000008.10:g.129542141A>G , CM000670.1:g.129542141A>G GRCh37
NC_000008.9:g.129611323A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+31175T>C
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