Canonical Allele Identifier: CA78941412

Gene: LINC02070

Linked Data

• dbSNP Id: rs1043340531
• gnomAD v2: 3-86544535-G-T
• gnomAD v3: 3-86495385-G-T
• gnomAD v4: 3-86495385-G-T
• MyVariant Identifiers: chr3:g.86544535G>T (hg19) ; chr3:g.86495385G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.86495385G>T , CM000665.2:g.86495385G>T	GRCh38
NC_000003.11:g.86544535G>T , CM000665.1:g.86544535G>T	GRCh37
NC_000003.10:g.86627225G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_245082.1:n.116-406G>T
NR_135563.1:n.116-406G>T