Canonical Allele Identifier: CA2355183501
Gene: LINC01432 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22057016C= , CM000682.2:g.22057016C= GRCh38
NC_000020.10:g.22037654C= , CM000682.1:g.22037654C= GRCh37
NC_000020.9:g.21985654C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.195+2732C=