Canonical Allele Identifier: CA585122910

Gene: LINC00824

Linked Data

• dbSNP Id: rs1417073967
• gnomAD v2: 8-129559124-G-C
• gnomAD v3: 8-128546878-G-C
• gnomAD v4: 8-128546878-G-C
• MyVariant Identifiers: chr8:g.129559124G>C (hg19) ; chr8:g.128546878G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128546878G>C , CM000670.2:g.128546878G>C	GRCh38
NC_000008.10:g.129559124G>C , CM000670.1:g.129559124G>C	GRCh37
NC_000008.9:g.129628306G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_121672.1:n.508+14192C>G