Canonical Allele Identifier: CA890035933
Gene: LINC02819 HGNC NCBI

Linked Data

dbSNP Id: rs1231513374
gnomAD v3: 1-159484124-A-T
gnomAD v4: 1-159484124-A-T
MyVariant Identifiers: chr1:g.159453914A>T (hg19) chr1:g.159484124A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159484124A>T , CM000663.2:g.159484124A>T GRCh38
NC_000001.10:g.159453914A>T , CM000663.1:g.159453914A>T GRCh37
NC_000001.9:g.157720538A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922189.1:n.678+1140A>T
XR_922189.3:n.690+1140A>T
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