Canonical Allele Identifier: CA911527594

Gene: LINC02070

Linked Data

• dbSNP Id: rs1387202767
• MyVariant Identifiers: chr3:g.86544541C>G (hg19) ; chr3:g.86495391C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.86495391C>G , CM000665.2:g.86495391C>G	GRCh38
NC_000003.11:g.86544541C>G , CM000665.1:g.86544541C>G	GRCh37
NC_000003.10:g.86627231C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_245082.1:n.116-400C>G
NR_135563.1:n.116-400C>G