Canonical Allele Identifier: CA1016157217
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs2054078180
gnomAD v3: 20-22059158-T-C
gnomAD v4: 20-22059158-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22059158T>C , CM000682.2:g.22059158T>C GRCh38
NC_000020.10:g.22039796T>C , CM000682.1:g.22039796T>C GRCh37
NC_000020.9:g.21987796T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.195+4874T>C
Search 100 bp 5'
Search 100 bp 3'