Canonical Allele Identifier: CA2815543197
Gene: LINC01432 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070161A>T , CM000682.2:g.22070161A>T GRCh38
NC_000020.10:g.22050799A>T , CM000682.1:g.22050799A>T GRCh37
NC_000020.9:g.21998799A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1473A>T
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