Canonical Allele Identifier: CA2355189663
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1982729945

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070108_22070109dup , CM000682.2:g.22070108_22070109dup GRCh38
NC_000020.10:g.22050746_22050747dup , CM000682.1:g.22050746_22050747dup GRCh37
NC_000020.9:g.21998746_21998747dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1420_445+1421dup