Canonical Allele Identifier: CA2355189692
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs8120846
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070140T>A , CM000682.2:g.22070140T>A GRCh38
NC_000020.10:g.22050778T>A , CM000682.1:g.22050778T>A GRCh37
NC_000020.9:g.21998778T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1452T>A
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