Canonical Allele Identifier: CA2355184626
Gene: LINC01432 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22059263T= , CM000682.2:g.22059263T= GRCh38
NC_000020.10:g.22039901T= , CM000682.1:g.22039901T= GRCh37
NC_000020.9:g.21987901T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038394.1:n.195+4979T=