Canonical Allele Identifier: CA2355189689
Gene: LINC01432 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070137A= , CM000682.2:g.22070137A= GRCh38
NC_000020.10:g.22050775A= , CM000682.1:g.22050775A= GRCh37
NC_000020.9:g.21998775A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1449A=