Canonical Allele Identifier: CA2063275067
Gene: LINC02356 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111398944G= , CM000674.2:g.111398944G= GRCh38
NC_000012.11:g.111836748G= , CM000674.1:g.111836748G= GRCh37
NC_000012.10:g.110321131G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945342.1:n.44+2071G=