Canonical Allele Identifier: CA2355189458
Gene: LINC01432 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22069711C= , CM000682.2:g.22069711C= GRCh38
NC_000020.10:g.22050349C= , CM000682.1:g.22050349C= GRCh37
NC_000020.9:g.21998349C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1023C=