Canonical Allele Identifier: CA2355189475
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1982720807

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22069754T>C , CM000682.2:g.22069754T>C GRCh38
NC_000020.10:g.22050392T>C , CM000682.1:g.22050392T>C GRCh37
NC_000020.9:g.21998392T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1066T>C