Canonical Allele Identifier: CA2355189469
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1889975021
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22069735A>C , CM000682.2:g.22069735A>C GRCh38
NC_000020.10:g.22050373A>C , CM000682.1:g.22050373A>C GRCh37
NC_000020.9:g.21998373A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1047A>C
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