Canonical Allele Identifier: CA2063275091
Gene: LINC02356 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111398975A= , CM000674.2:g.111398975A= GRCh38
NC_000012.11:g.111836779A= , CM000674.1:g.111836779A= GRCh37
NC_000012.10:g.110321162A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945342.1:n.44+2102A=