Canonical Allele Identifier: CA2355189652
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1982729312

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070084_22070086dup , CM000682.2:g.22070084_22070086dup GRCh38
NC_000020.10:g.22050722_22050724dup , CM000682.1:g.22050722_22050724dup GRCh37
NC_000020.9:g.21998722_21998724dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1396_445+1398dup