Canonical Allele Identifier: CA607341393
Gene: LINC02356 HGNC NCBI

Linked Data

dbSNP Id: rs1349626605

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111399010T>C , CM000674.2:g.111399010T>C GRCh38
NC_000012.11:g.111836814T>C , CM000674.1:g.111836814T>C GRCh37
NC_000012.10:g.110321197T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945342.1:n.44+2137T>C