Canonical Allele Identifier: CA585122937

Gene: LINC00824

Linked Data

• dbSNP Id: rs1396505987
• gnomAD v2: 8-129559373-C-A
• gnomAD v3: 8-128547127-C-A
• gnomAD v4: 8-128547127-C-A
• MyVariant Identifiers: chr8:g.129559373C>A (hg19) ; chr8:g.128547127C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.128547127C>A , CM000670.2:g.128547127C>A	GRCh38
NC_000008.10:g.129559373C>A , CM000670.1:g.129559373C>A	GRCh37
NC_000008.9:g.129628555C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_121672.1:n.508+13943G>T