Canonical Allele Identifier: CA2355189571
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1600438701

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22069918G>A , CM000682.2:g.22069918G>A GRCh38
NC_000020.10:g.22050556G>A , CM000682.1:g.22050556G>A GRCh37
NC_000020.9:g.21998556G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1230G>A