Canonical Allele Identifier: CA301355850
Gene: LINC02565 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.57316323G>T , CM000680.2:g.57316323G>T GRCh38
NC_000018.9:g.54983554G>T , CM000680.1:g.54983554G>T GRCh37
NC_000018.8:g.53134552G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935518.1:n.203+17807C>A