Canonical Allele Identifier: CA2355189596
Gene: LINC01432 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22069975C= , CM000682.2:g.22069975C= GRCh38
NC_000020.10:g.22050613C= , CM000682.1:g.22050613C= GRCh37
NC_000020.9:g.21998613C= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038394.1:n.445+1287C=