Canonical Allele Identifier: CA89646426

Gene: LINC02043

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186812695T>G , CM000665.2:g.186812695T>G	GRCh38
NC_000003.11:g.186530484T>G , CM000665.1:g.186530484T>G	GRCh37
NC_000003.10:g.188013178T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_125409.1:n.564-547A>C