Canonical Allele Identifier: CA89646393

Gene: LINC02043

Linked Data

• dbSNP Id: rs1052534971
• MyVariant Identifiers: chr3:g.186530429C>T (hg19) ; chr3:g.186812640C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186812640C>T , CM000665.2:g.186812640C>T	GRCh38
NC_000003.11:g.186530429C>T , CM000665.1:g.186530429C>T	GRCh37
NC_000003.10:g.188013123C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_125409.1:n.564-492G>A