Canonical Allele Identifier: CA1201917060
Gene: LINC02819 HGNC NCBI

Linked Data

dbSNP Id: rs1656898846
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159484215T>C , CM000663.2:g.159484215T>C GRCh38
NC_000001.10:g.159454005T>C , CM000663.1:g.159454005T>C GRCh37
NC_000001.9:g.157720629T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922189.1:n.678+1231T>C
XR_922189.3:n.690+1231T>C
Search 100 bp 5'
Search 100 bp 3'