Canonical Allele Identifier: CA544492187

Gene: LINC02070

Linked Data

• dbSNP Id: rs1457886916
• gnomAD v2: 3-86544472-A-T
• gnomAD v3: 3-86495322-A-T
• gnomAD v4: 3-86495322-A-T
• MyVariant Identifiers: chr3:g.86544472A>T (hg19) ; chr3:g.86495322A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.86495322A>T , CM000665.2:g.86495322A>T	GRCh38
NC_000003.11:g.86544472A>T , CM000665.1:g.86544472A>T	GRCh37
NC_000003.10:g.86627162A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_245082.1:n.116-469A>T
NR_135563.1:n.116-469A>T