Canonical Allele Identifier: CA2355183502
Gene: LINC01432 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22057017C= , CM000682.2:g.22057017C= GRCh38
NC_000020.10:g.22037655C= , CM000682.1:g.22037655C= GRCh37
NC_000020.9:g.21985655C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.195+2733C=