Canonical Allele Identifier: CA951840631
Gene: LINC02356 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111399067A>C , CM000674.2:g.111399067A>C GRCh38
NC_000012.11:g.111836871A>C , CM000674.1:g.111836871A>C GRCh37
NC_000012.10:g.110321254A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945342.1:n.44+2194A>C