Canonical Allele Identifier: CA2355189489
Gene: LINC01432 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22069774C= , CM000682.2:g.22069774C= GRCh38
NC_000020.10:g.22050412C= , CM000682.1:g.22050412C= GRCh37
NC_000020.9:g.21998412C= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038394.1:n.445+1086C=