Canonical Allele Identifier: CA2797467369
Gene: LINC02356 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111399124C>T , CM000674.2:g.111399124C>T GRCh38
NC_000012.11:g.111836928C>T , CM000674.1:g.111836928C>T GRCh37
NC_000012.10:g.110321311C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945342.1:n.44+2251C>T