Canonical Allele Identifier: CA2815543196
Gene: LINC01432 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070155T>A , CM000682.2:g.22070155T>A GRCh38
NC_000020.10:g.22050793T>A , CM000682.1:g.22050793T>A GRCh37
NC_000020.9:g.21998793T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1467T>A