Canonical Allele Identifier: CA526647872

Gene: LINC02819

Linked Data

• dbSNP Id: rs1281275109
• gnomAD v2: 1-159454030-C-T
• gnomAD v3: 1-159484240-C-T
• gnomAD v4: 1-159484240-C-T
• MyVariant Identifiers: chr1:g.159454030C>T (hg19) ; chr1:g.159484240C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159484240C>T , CM000663.2:g.159484240C>T	GRCh38
NC_000001.10:g.159454030C>T , CM000663.1:g.159454030C>T	GRCh37
NC_000001.9:g.157720654C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_922189.1:n.678+1256C>T
XR_922189.3:n.690+1256C>T