Canonical Allele Identifier: CA2355189675
Gene: LINC01432 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070115T= , CM000682.2:g.22070115T= GRCh38
NC_000020.10:g.22050753T= , CM000682.1:g.22050753T= GRCh37
NC_000020.9:g.21998753T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1427T=