Canonical Allele Identifier: CA2355183489
Gene: LINC01432 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22056983A= , CM000682.2:g.22056983A= GRCh38
NC_000020.10:g.22037621A= , CM000682.1:g.22037621A= GRCh37
NC_000020.9:g.21985621A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038394.1:n.195+2699A=