Canonical Allele Identifier: CA1201917067
Gene: LINC02819 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159484226_159484227delinsAT , CM000663.2:g.159484226_159484227delinsAT GRCh38
NC_000001.10:g.159454016_159454017delinsAT , CM000663.1:g.159454016_159454017delinsAT GRCh37
NC_000001.9:g.157720640_157720641delinsAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922189.1:n.678+1242_678+1243delinsAT
XR_922189.3:n.690+1242_690+1243delinsAT