Canonical Allele Identifier: CA2355189465
Gene: LINC01432 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22069728G= , CM000682.2:g.22069728G= GRCh38
NC_000020.10:g.22050366G= , CM000682.1:g.22050366G= GRCh37
NC_000020.9:g.21998366G= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038394.1:n.445+1040G=