Canonical Allele Identifier: CA1016158391
Gene: LINC01432 HGNC NCBI
gnomAD v3:
20:22061780 A / T
gnomAD v4:
chr20-22061780-A-T
Joint Max Group AF 0.00001973 (NFE)
Genomes Max Group AF 0.00001973 (NFE)
dbSNP:
913063
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22061780A>T , CM000682.2:g.22061780A>T GRCh38
NC_000020.10:g.22042418A>T , CM000682.1:g.22042418A>T GRCh37
NC_000020.9:g.21990418A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.196-6659A>T
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