Canonical Allele Identifier: CA607341389

Gene: LINC02356

Linked Data

• dbSNP Id: rs1397150878
• gnomAD v2: 12-111836719-C-T
• gnomAD v3: 12-111398915-C-T
• gnomAD v4: 12-111398915-C-T
• MyVariant Identifiers: chr12:g.111836719C>T (hg19) ; chr12:g.111398915C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.111398915C>T , CM000674.2:g.111398915C>T	GRCh38
NC_000012.11:g.111836719C>T , CM000674.1:g.111836719C>T	GRCh37
NC_000012.10:g.110321102C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_945342.1:n.44+2042C>T