Canonical Allele Identifier: CA635116533
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1265012037
gnomAD v2: 20-22039877-T-C
gnomAD v3: 20-22059239-T-C
gnomAD v4: 20-22059239-T-C
MyVariant Identifiers: chr20:g.22039877T>C (hg19) chr20:g.22059239T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22059239T>C , CM000682.2:g.22059239T>C GRCh38
NC_000020.10:g.22039877T>C , CM000682.1:g.22039877T>C GRCh37
NC_000020.9:g.21987877T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038394.1:n.195+4955T>C
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