Canonical Allele Identifier: CA31223078
Gene: LINC02819 HGNC NCBI

Linked Data

dbSNP Id: rs913405263
gnomAD v2: 1-159453927-A-C
gnomAD v3: 1-159484137-A-C
gnomAD v4: 1-159484137-A-C
MyVariant Identifiers: chr1:g.159453927A>C (hg19) chr1:g.159484137A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159484137A>C , CM000663.2:g.159484137A>C GRCh38
NC_000001.10:g.159453927A>C , CM000663.1:g.159453927A>C GRCh37
NC_000001.9:g.157720551A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922189.1:n.678+1153A>C
XR_922189.3:n.690+1153A>C
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