Canonical Allele Identifier: CA89646466

Gene: LINC02043

Linked Data

• dbSNP Id: rs1031000612
• MyVariant Identifiers: chr3:g.186530511A>G (hg19) ; chr3:g.186812722A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186812722A>G , CM000665.2:g.186812722A>G	GRCh38
NC_000003.11:g.186530511A>G , CM000665.1:g.186530511A>G	GRCh37
NC_000003.10:g.188013205A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_125409.1:n.564-574T>C