Canonical Allele Identifier: CA2815543195
Gene: LINC01432 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070154G>C , CM000682.2:g.22070154G>C GRCh38
NC_000020.10:g.22050792G>C , CM000682.1:g.22050792G>C GRCh37
NC_000020.9:g.21998792G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1466G>C