Canonical Allele Identifier: CA1016142494
Gene: LINC01432 HGNC NCBI

Linked Data

gnomAD v3: 20-22070139-A-C
gnomAD v4: 20-22070139-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070139A>C , CM000682.2:g.22070139A>C GRCh38
NC_000020.10:g.22050777A>C , CM000682.1:g.22050777A>C GRCh37
NC_000020.9:g.21998777A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1451A>C
Search 100 bp 5'
Search 100 bp 3'