Canonical Allele Identifier: CA951840628
Gene: LINC02356 HGNC NCBI

Linked Data

dbSNP Id: rs1869952503

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111399053A>G , CM000674.2:g.111399053A>G GRCh38
NC_000012.11:g.111836857A>G , CM000674.1:g.111836857A>G GRCh37
NC_000012.10:g.110321240A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945342.1:n.44+2180A>G