Canonical Allele Identifier: CA2063275001
Gene: LINC02356 HGNC NCBI

Linked Data

dbSNP Id: rs781744804

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111398812G>C , CM000674.2:g.111398812G>C GRCh38
NC_000012.11:g.111836616G>C , CM000674.1:g.111836616G>C GRCh37
NC_000012.10:g.110320999G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945342.1:n.44+1939G>C