Canonical Allele Identifier: CA2355189681
Gene: LINC01432 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070128T= , CM000682.2:g.22070128T= GRCh38
NC_000020.10:g.22050766T= , CM000682.1:g.22050766T= GRCh37
NC_000020.9:g.21998766T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1440T=