Canonical Allele Identifier: CA2355184606
Gene: LINC01432 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22059229T= , CM000682.2:g.22059229T= GRCh38
NC_000020.10:g.22039867T= , CM000682.1:g.22039867T= GRCh37
NC_000020.9:g.21987867T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.195+4945T=