Canonical Allele Identifier: CA2063275130
Gene: LINC02356 HGNC NCBI

Linked Data

dbSNP Id: rs539085363
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111399106G>A , CM000674.2:g.111399106G>A GRCh38
NC_000012.11:g.111836910G>A , CM000674.1:g.111836910G>A GRCh37
NC_000012.10:g.110321293G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945342.1:n.44+2233G>A
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