Canonical Allele Identifier: CA2355189594
Gene: LINC01432 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22069974T= , CM000682.2:g.22069974T= GRCh38
NC_000020.10:g.22050612T= , CM000682.1:g.22050612T= GRCh37
NC_000020.9:g.21998612T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1286T=