Canonical Allele Identifier: CA78941410

Gene: LINC02070

Linked Data

• dbSNP Id: rs910545520
• gnomAD v2: 3-86544503-A-G
• gnomAD v3: 3-86495353-A-G
• gnomAD v4: 3-86495353-A-G
• MyVariant Identifiers: chr3:g.86544503A>G (hg19) ; chr3:g.86495353A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.86495353A>G , CM000665.2:g.86495353A>G	GRCh38
NC_000003.11:g.86544503A>G , CM000665.1:g.86544503A>G	GRCh37
NC_000003.10:g.86627193A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_245082.1:n.116-438A>G
NR_135563.1:n.116-438A>G