Canonical Allele Identifier: CA1016142081
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1982726034
gnomAD v3: 20-22069940-C-G
gnomAD v4: 20-22069940-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22069940C>G , CM000682.2:g.22069940C>G GRCh38
NC_000020.10:g.22050578C>G , CM000682.1:g.22050578C>G GRCh37
NC_000020.9:g.21998578C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038394.1:n.445+1252C>G
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