Canonical Allele Identifier: CA1016142437
Gene: LINC01432 HGNC NCBI

Linked Data

gnomAD v3: 20-22070134-T-TTTG
gnomAD v4: 20-22070134-T-TTTG
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070135_22070136insTGT , CM000682.2:g.22070135_22070136insTGT GRCh38
NC_000020.10:g.22050773_22050774insTGT , CM000682.1:g.22050773_22050774insTGT GRCh37
NC_000020.9:g.21998773_21998774insTGT NCBI36

Transcript Alleles

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