Canonical Allele Identifier: CA2355189671
Gene: LINC01432 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070113C= , CM000682.2:g.22070113C= GRCh38
NC_000020.10:g.22050751C= , CM000682.1:g.22050751C= GRCh37
NC_000020.9:g.21998751C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1425C=