Canonical Allele Identifier: CA914598638
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1568576817
gnomAD v2: 20-22050750-T-G
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1424T>G
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