Canonical Allele Identifier: CA2815543136
Gene: LINC01432 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22069664G>A , CM000682.2:g.22069664G>A GRCh38
NC_000020.10:g.22050302G>A , CM000682.1:g.22050302G>A GRCh37
NC_000020.9:g.21998302G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+976G>A