Canonical Allele Identifier: CA1016142392
Gene: LINC01432 HGNC NCBI

Linked Data

gnomAD v3: 20-22070113-C-CTTTTTTTTTTTTTTTTTTTTTTTTTTTT
gnomAD v4: 20-22070113-C-CTTTTTTTTTTTTTTTTTTTTTTTTTTTT
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070135_22070136insTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000682.2:g.22070135_22070136insTTTTTTTTTTTTTTTTTTTTTTTTTTTT GRCh38
NC_000020.10:g.22050773_22050774insTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000682.1:g.22050773_22050774insTTTTTTTTTTTTTTTTTTTTTTTTTTTT GRCh37
NC_000020.9:g.21998773_21998774insTTTTTTTTTTTTTTTTTTTTTTTTTTTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1447_445+1448insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Search 100 bp 5'
Search 100 bp 3'