Canonical Allele Identifier: CA544492126

Gene: LINC02070

Linked Data

• dbSNP Id: rs1222957841
• gnomAD v2: 3-86544437-A-G
• gnomAD v3: 3-86495287-A-G
• gnomAD v4: 3-86495287-A-G
• MyVariant Identifiers: chr3:g.86544437A>G (hg19) ; chr3:g.86495287A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.86495287A>G , CM000665.2:g.86495287A>G	GRCh38
NC_000003.11:g.86544437A>G , CM000665.1:g.86544437A>G	GRCh37
NC_000003.10:g.86627127A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_245082.1:n.116-504A>G
NR_135563.1:n.116-504A>G