Canonical Allele Identifier: CA2063275060
Gene: LINC02356 HGNC NCBI

Linked Data

dbSNP Id: rs1869949886

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111398933C>A , CM000674.2:g.111398933C>A GRCh38
NC_000012.11:g.111836737C>A , CM000674.1:g.111836737C>A GRCh37
NC_000012.10:g.110321120C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945342.1:n.44+2060C>A