Canonical Allele Identifier: CA31223075
Gene: LINC02819 HGNC NCBI

Linked Data

dbSNP Id: rs557752283
gnomAD v3: 1-159484106-G-C
gnomAD v4: 1-159484106-G-C
MyVariant Identifiers: chr1:g.159453896G>C (hg19) chr1:g.159484106G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159484106G>C , CM000663.2:g.159484106G>C GRCh38
NC_000001.10:g.159453896G>C , CM000663.1:g.159453896G>C GRCh37
NC_000001.9:g.157720520G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922189.1:n.678+1122G>C
XR_922189.3:n.690+1122G>C
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