Canonical Allele Identifier: CA1016142033
Gene: LINC01432 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22069836A>C , CM000682.2:g.22069836A>C GRCh38
NC_000020.10:g.22050474A>C , CM000682.1:g.22050474A>C GRCh37
NC_000020.9:g.21998474A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038394.1:n.445+1148A>C