Canonical Allele Identifier: CA2355184614
Gene: LINC01432 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22059239T= , CM000682.2:g.22059239T= GRCh38
NC_000020.10:g.22039877T= , CM000682.1:g.22039877T= GRCh37
NC_000020.9:g.21987877T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038394.1:n.195+4955T=