Canonical Allele Identifier: CA890035905
Gene: LINC02819 HGNC NCBI

Linked Data

dbSNP Id: rs1164162491
gnomAD v3: 1-159484087-C-T
gnomAD v4: 1-159484087-C-T
MyVariant Identifiers: chr1:g.159453877C>T (hg19) chr1:g.159484087C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159484087C>T , CM000663.2:g.159484087C>T GRCh38
NC_000001.10:g.159453877C>T , CM000663.1:g.159453877C>T GRCh37
NC_000001.9:g.157720501C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922189.1:n.678+1103C>T
XR_922189.3:n.690+1103C>T
Search 100 bp 5'
Search 100 bp 3'