Canonical Allele Identifier: CA635117069
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1340140648
gnomAD v2: 20-22050294-G-A
gnomAD v3: 20-22069656-G-A
gnomAD v4: 20-22069656-G-A
MyVariant Identifiers: chr20:g.22050294G>A (hg19) chr20:g.22069656G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22069656G>A , CM000682.2:g.22069656G>A GRCh38
NC_000020.10:g.22050294G>A , CM000682.1:g.22050294G>A GRCh37
NC_000020.9:g.21998294G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+968G>A
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