Canonical Allele Identifier: CA185876347

Gene: LINC00824

Linked Data

• dbSNP Id: rs1008964573
• gnomAD v2: 8-129559154-T-C
• gnomAD v3: 8-128546908-T-C
• gnomAD v4: 8-128546908-T-C
• MyVariant Identifiers: chr8:g.129559154T>C (hg19) ; chr8:g.128546908T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128546908T>C , CM000670.2:g.128546908T>C	GRCh38
NC_000008.10:g.129559154T>C , CM000670.1:g.129559154T>C	GRCh37
NC_000008.9:g.129628336T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_121672.1:n.508+14162A>G