Canonical Allele Identifier: CA89646452

Gene: LINC02043

Linked Data

• dbSNP Id: rs538226299
• gnomAD v2: 3-186530485-G-A
• gnomAD v3: 3-186812696-G-A
• gnomAD v4: 3-186812696-G-A
• MyVariant Identifiers: chr3:g.186530485G>A (hg19) ; chr3:g.186812696G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186812696G>A , CM000665.2:g.186812696G>A	GRCh38
NC_000003.11:g.186530485G>A , CM000665.1:g.186530485G>A	GRCh37
NC_000003.10:g.188013179G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_125409.1:n.564-548C>T