Canonical Allele Identifier: CA1016142401
Gene: LINC01432 HGNC NCBI

Linked Data

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

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070135_22070136insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000682.2:g.22070135_22070136insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT GRCh38
NC_000020.10:g.22050773_22050774insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000682.1:g.22050773_22050774insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT GRCh37
NC_000020.9:g.21998773_21998774insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NCBI36

Transcript Alleles

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