Canonical Allele Identifier: CA2355189447
Gene: LINC01432 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22069685C= , CM000682.2:g.22069685C= GRCh38
NC_000020.10:g.22050323C= , CM000682.1:g.22050323C= GRCh37
NC_000020.9:g.21998323C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+997C=