Canonical Allele Identifier: CA1016142175
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs200737996
gnomAD v3: 20-22070113-C-A
gnomAD v4: 20-22070113-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070113C>A , CM000682.2:g.22070113C>A GRCh38
NC_000020.10:g.22050751C>A , CM000682.1:g.22050751C>A GRCh37
NC_000020.9:g.21998751C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1425C>A
Search 100 bp 5'
Search 100 bp 3'