Canonical Allele Identifier: CA89646478

Gene: LINC02043

Linked Data

• dbSNP Id: rs993571225
• gnomAD v2: 3-186530530-G-A
• gnomAD v3: 3-186812741-G-A
• gnomAD v4: 3-186812741-G-A
• MyVariant Identifiers: chr3:g.186530530G>A (hg19) ; chr3:g.186812741G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186812741G>A , CM000665.2:g.186812741G>A	GRCh38
NC_000003.11:g.186530530G>A , CM000665.1:g.186530530G>A	GRCh37
NC_000003.10:g.188013224G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_125409.1:n.564-593C>T