Canonical Allele Identifier: CA2355189454
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1600438607
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22069692A>G , CM000682.2:g.22069692A>G GRCh38
NC_000020.10:g.22050330A>G , CM000682.1:g.22050330A>G GRCh37
NC_000020.9:g.21998330A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1004A>G
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