Canonical Allele Identifier: CA607341390

Gene: LINC02356

Linked Data

• dbSNP Id: rs1435674598
• gnomAD v2: 12-111836722-T-C
• gnomAD v3: 12-111398918-T-C
• gnomAD v4: 12-111398918-T-C
• MyVariant Identifiers: chr12:g.111836722T>C (hg19) ; chr12:g.111398918T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.111398918T>C , CM000674.2:g.111398918T>C	GRCh38
NC_000012.11:g.111836722T>C , CM000674.1:g.111836722T>C	GRCh37
NC_000012.10:g.110321105T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_945342.1:n.44+2045T>C