Canonical Allele Identifier: CA89646365

Gene: LINC02043

Linked Data

• dbSNP Id: rs144178947
• gnomAD v3: 3-186812626-C-G
• gnomAD v4: 3-186812626-C-G
• MyVariant Identifiers: chr3:g.186530415C>G (hg19) ; chr3:g.186812626C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186812626C>G , CM000665.2:g.186812626C>G	GRCh38
NC_000003.11:g.186530415C>G , CM000665.1:g.186530415C>G	GRCh37
NC_000003.10:g.188013109C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_125409.1:n.564-478G>C