Canonical Allele Identifier: CA2518963628
Gene: LINC01432 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070114_22070115insC , CM000682.2:g.22070114_22070115insC GRCh38
NC_000020.10:g.22050752_22050753insC , CM000682.1:g.22050752_22050753insC GRCh37
NC_000020.9:g.21998752_21998753insC NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1426_445+1427insC