Canonical Allele Identifier: CA526647853
Gene: LINC02819 HGNC NCBI

Linked Data

dbSNP Id: rs1322172171
gnomAD v2: 1-159453889-C-A
gnomAD v3: 1-159484099-C-A
gnomAD v4: 1-159484099-C-A
MyVariant Identifiers: chr1:g.159453889C>A (hg19) chr1:g.159484099C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159484099C>A , CM000663.2:g.159484099C>A GRCh38
NC_000001.10:g.159453889C>A , CM000663.1:g.159453889C>A GRCh37
NC_000001.9:g.157720513C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922189.1:n.678+1115C>A
XR_922189.3:n.690+1115C>A
Search 100 bp 5'
Search 100 bp 3'