Canonical Allele Identifier: CA2355189431
Gene: LINC01432 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22069658A= , CM000682.2:g.22069658A= GRCh38
NC_000020.10:g.22050296A= , CM000682.1:g.22050296A= GRCh37
NC_000020.9:g.21998296A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+970A=