Canonical Allele Identifier: CA89646413
Gene: LINC02043 HGNC NCBI

Linked Data

dbSNP Id: rs946648738
gnomAD v2: 3-186530468-C-T
gnomAD v3: 3-186812679-C-T
gnomAD v4: 3-186812679-C-T
MyVariant Identifiers: chr3:g.186530468C>T (hg19) chr3:g.186812679C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186812679C>T , CM000665.2:g.186812679C>T GRCh38
NC_000003.11:g.186530468C>T , CM000665.1:g.186530468C>T GRCh37
NC_000003.10:g.188013162C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125409.1:n.564-531G>A
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