Canonical Allele Identifier: CA437379978
Gene: LINC02043 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.186530449del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186812661del , CM000665.2:g.186812661del GRCh38
NC_000003.11:g.186530450del , CM000665.1:g.186530450del GRCh37
NC_000003.10:g.188013144del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125409.1:n.564-512del