Canonical Allele Identifier: CA1008293284
Gene: LINC02819 HGNC NCBI

Linked Data

dbSNP Id: rs1656896312
gnomAD v3: 1-159484079-G-A
gnomAD v4: 1-159484079-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159484079G>A , CM000663.2:g.159484079G>A GRCh38
NC_000001.10:g.159453869G>A , CM000663.1:g.159453869G>A GRCh37
NC_000001.9:g.157720493G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922189.1:n.678+1095G>A
XR_922189.3:n.690+1095G>A
Search 100 bp 5'
Search 100 bp 3'