Canonical Allele Identifier: CA683615311
Gene: LINC02356 HGNC NCBI

Linked Data

dbSNP Id: rs1230097400

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111398979T>C , CM000674.2:g.111398979T>C GRCh38
NC_000012.11:g.111836783T>C , CM000674.1:g.111836783T>C GRCh37
NC_000012.10:g.110321166T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945342.1:n.44+2106T>C