Canonical Allele Identifier: CA2355189664
Gene: LINC01432 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070109_22070112delinsGCTT , CM000682.2:g.22070109_22070112delinsGCTT GRCh38
NC_000020.10:g.22050747_22050750delinsGCTT , CM000682.1:g.22050747_22050750delinsGCTT GRCh37
NC_000020.9:g.21998747_21998750delinsGCTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1421_445+1424delinsGCTT
Search 100 bp 5'
Search 100 bp 3'