Canonical Allele Identifier: CA2355189538
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1600438669

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22069846C>A , CM000682.2:g.22069846C>A GRCh38
NC_000020.10:g.22050484C>A , CM000682.1:g.22050484C>A GRCh37
NC_000020.9:g.21998484C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1158C>A