Canonical Allele Identifier: CA657568296
Gene: LINC01432 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22069662G>T , CM000682.2:g.22069662G>T GRCh38
NC_000020.10:g.22050300G>T , CM000682.1:g.22050300G>T GRCh37
NC_000020.9:g.21998300G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+974G>T