Canonical Allele Identifier: CA243588873

Gene: LINC02356

Linked Data

• dbSNP Id: rs149474059
• gnomAD v2: 12-111836738-C-A
• gnomAD v3: 12-111398934-C-A
• gnomAD v4: 12-111398934-C-A
• MyVariant Identifiers: chr12:g.111836738C>A (hg19) ; chr12:g.111398934C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.111398934C>A , CM000674.2:g.111398934C>A	GRCh38
NC_000012.11:g.111836738C>A , CM000674.1:g.111836738C>A	GRCh37
NC_000012.10:g.110321121C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_945342.1:n.44+2061C>A