Canonical Allele Identifier: CA78941387

Gene: LINC02070

Linked Data

• dbSNP Id: rs113607646
• gnomAD v2: 3-86544398-T-G
• gnomAD v3: 3-86495248-T-G
• gnomAD v4: 3-86495248-T-G
• MyVariant Identifiers: chr3:g.86544398T>G (hg19) ; chr3:g.86495248T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.86495248T>G , CM000665.2:g.86495248T>G	GRCh38
NC_000003.11:g.86544398T>G , CM000665.1:g.86544398T>G	GRCh37
NC_000003.10:g.86627088T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_245082.1:n.116-543T>G
NR_135563.1:n.116-543T>G