Canonical Allele Identifier: CA1016157268
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1982465507
gnomAD v3: 20-22059233-T-C
gnomAD v4: 20-22059233-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22059233T>C , CM000682.2:g.22059233T>C GRCh38
NC_000020.10:g.22039871T>C , CM000682.1:g.22039871T>C GRCh37
NC_000020.9:g.21987871T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038394.1:n.195+4949T>C
Search 100 bp 5'
Search 100 bp 3'