Canonical Allele Identifier: CA2815543166
Gene: LINC01432 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22069932A>G , CM000682.2:g.22069932A>G GRCh38
NC_000020.10:g.22050570A>G , CM000682.1:g.22050570A>G GRCh37
NC_000020.9:g.21998570A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038394.1:n.445+1244A>G