Canonical Allele Identifier: CA1016142341
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs397865655

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070128_22070135dup , CM000682.2:g.22070128_22070135dup GRCh38
NC_000020.10:g.22050766_22050773dup , CM000682.1:g.22050766_22050773dup GRCh37
NC_000020.9:g.21998766_21998773dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1440_445+1447dup