Canonical Allele Identifier: CA890036059

Gene: LINC02819

Linked Data

• dbSNP Id: rs1192300258
• gnomAD v3: 1-159484213-C-A
• gnomAD v4: 1-159484213-C-A
• MyVariant Identifiers: chr1:g.159454003C>A (hg19) ; chr1:g.159484213C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159484213C>A , CM000663.2:g.159484213C>A	GRCh38
NC_000001.10:g.159454003C>A , CM000663.1:g.159454003C>A	GRCh37
NC_000001.9:g.157720627C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_922189.1:n.678+1229C>A
XR_922189.3:n.690+1229C>A