Canonical Allele Identifier: CA2355189444
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1982719509

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22069680A>C , CM000682.2:g.22069680A>C GRCh38
NC_000020.10:g.22050318A>C , CM000682.1:g.22050318A>C GRCh37
NC_000020.9:g.21998318A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+992A>C