Canonical Allele Identifier: CA607341395

Gene: LINC02356

Linked Data

• dbSNP Id: rs1279391373
• gnomAD v2: 12-111836905-A-G
• MyVariant Identifiers: chr12:g.111836905A>G (hg19) ; chr12:g.111399101A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.111399101A>G , CM000674.2:g.111399101A>G	GRCh38
NC_000012.11:g.111836905A>G , CM000674.1:g.111836905A>G	GRCh37
NC_000012.10:g.110321288A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_945342.1:n.44+2228A>G