Canonical Allele Identifier: CA1016157271
Gene: LINC01432 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22059236G>A , CM000682.2:g.22059236G>A GRCh38
NC_000020.10:g.22039874G>A , CM000682.1:g.22039874G>A GRCh37
NC_000020.9:g.21987874G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038394.1:n.195+4952G>A