Canonical Allele Identifier: CA2747678820
Gene: LINC02775 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214087739C>A , CM000663.2:g.214087739C>A GRCh38
NC_000001.10:g.214261082C>A , CM000663.1:g.214261082C>A GRCh37
NC_000001.9:g.212327705C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510303.1:c.-188-15301G>T XP_011508605.1:n.-188-15301G>T
XR_922584.1:n.119-15301G>T
XR_922584.2:n.261-15301G>T
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