Canonical Allele Identifier: CA2355183522
Gene: LINC01432 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22057063T= , CM000682.2:g.22057063T= GRCh38
NC_000020.10:g.22037701T= , CM000682.1:g.22037701T= GRCh37
NC_000020.9:g.21985701T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.195+2779T=