Canonical Allele Identifier: CA510033499
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1555784632
gnomAD v2: 20-22050748-C-CT
gnomAD v3: 20-22070110-C-CT
gnomAD v4: 20-22070110-C-CT
MyVariant Identifiers: chr20:g.22050748_22050749insT (hg19) chr20:g.22070110_22070111insT (hg38)
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Genomic Alleles

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

Transcript Alleles

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