Canonical Allele Identifier: CA1427113030
Gene: LINC02043 HGNC NCBI

Linked Data

dbSNP Id: rs1018773350
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186812730G>A , CM000665.2:g.186812730G>A GRCh38
NC_000003.11:g.186530519G>A , CM000665.1:g.186530519G>A GRCh37
NC_000003.10:g.188013213G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125409.1:n.564-582C>T
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