Canonical Allele Identifier: CA2355189677
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1982730747
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070116T>C , CM000682.2:g.22070116T>C GRCh38
NC_000020.10:g.22050754T>C , CM000682.1:g.22050754T>C GRCh37
NC_000020.9:g.21998754T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1428T>C
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