Canonical Allele Identifier: CA89646362
Gene: LINC02043 HGNC NCBI

Linked Data

dbSNP Id: rs927736386
gnomAD v3: 3-186812613-C-T
gnomAD v4: 3-186812613-C-T
MyVariant Identifiers: chr3:g.186530402C>T (hg19) chr3:g.186812613C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186812613C>T , CM000665.2:g.186812613C>T GRCh38
NC_000003.11:g.186530402C>T , CM000665.1:g.186530402C>T GRCh37
NC_000003.10:g.188013096C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125409.1:n.564-465G>A
Search 100 bp 5'
Search 100 bp 3'