Canonical Allele Identifier: CA78941414

Gene: LINC02070

Linked Data

• dbSNP Id: rs80030395
• MyVariant Identifiers: chr3:g.86544549A>C (hg19) ; chr3:g.86495399A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.86495399A>C , CM000665.2:g.86495399A>C	GRCh38
NC_000003.11:g.86544549A>C , CM000665.1:g.86544549A>C	GRCh37
NC_000003.10:g.86627239A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_245082.1:n.116-392A>C
NR_135563.1:n.116-392A>C