Canonical Allele Identifier: CA2500257298
Gene: LINC01432 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070113_22070117del , CM000682.2:g.22070113_22070117del GRCh38
NC_000020.10:g.22050751_22050755del , CM000682.1:g.22050751_22050755del GRCh37
NC_000020.9:g.21998751_21998755del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1425_445+1429del