Canonical Allele Identifier: CA2815543170
Gene: LINC01432 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070094C>A , CM000682.2:g.22070094C>A GRCh38
NC_000020.10:g.22050732C>A , CM000682.1:g.22050732C>A GRCh37
NC_000020.9:g.21998732C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1406C>A
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