Canonical Allele Identifier: CA185876398

Gene: LINC00824

Linked Data

• dbSNP Id: rs145481795
• gnomAD v2: 8-129559520-G-C
• gnomAD v3: 8-128547274-G-C
• gnomAD v4: 8-128547274-G-C
• MyVariant Identifiers: chr8:g.129559520G>C (hg19) ; chr8:g.128547274G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128547274G>C , CM000670.2:g.128547274G>C	GRCh38
NC_000008.10:g.129559520G>C , CM000670.1:g.129559520G>C	GRCh37
NC_000008.9:g.129628702G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121672.1:n.508+13796C>G