Canonical Allele Identifier: CA646403919
Gene: LINC02775 HGNC NCBI

Linked Data

COSMIC: COSN5166150 COSN21888154
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214087800A>T , CM000663.2:g.214087800A>T GRCh38
NC_000001.10:g.214261143A>T , CM000663.1:g.214261143A>T GRCh37
NC_000001.9:g.212327766A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510303.1:c.-188-15362T>A XP_011508605.1:n.-188-15362T>A
XR_922584.1:n.119-15362T>A
XR_922584.2:n.261-15362T>A
Search 100 bp 5'
Search 100 bp 3'