Canonical Allele Identifier: CA2063275087
Gene: LINC02356 HGNC NCBI

Linked Data

dbSNP Id: rs1869951340

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111398970C>T , CM000674.2:g.111398970C>T GRCh38
NC_000012.11:g.111836774C>T , CM000674.1:g.111836774C>T GRCh37
NC_000012.10:g.110321157C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945342.1:n.44+2097C>T