Canonical Allele Identifier: CA2063275118
Gene: LINC02356 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111399067A= , CM000674.2:g.111399067A= GRCh38
NC_000012.11:g.111836871A= , CM000674.1:g.111836871A= GRCh37
NC_000012.10:g.110321254A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945342.1:n.44+2194A=