Canonical Allele Identifier: CA1016142152
Gene: LINC01432 HGNC NCBI

Linked Data

gnomAD v3: 20-22070110-C-CTTTT
gnomAD v4: 20-22070110-C-CTTTT
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070112_22070113insTTTT , CM000682.2:g.22070112_22070113insTTTT GRCh38
NC_000020.10:g.22050750_22050751insTTTT , CM000682.1:g.22050750_22050751insTTTT GRCh37
NC_000020.9:g.21998750_21998751insTTTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1424_445+1425insTTTT
Search 100 bp 5'
Search 100 bp 3'