Canonical Allele Identifier: CA313071478

Gene: LINC01432

Linked Data

• dbSNP Id: rs779207526
• gnomAD v3: 20-22059260-C-A
• gnomAD v4: 20-22059260-C-A
• MyVariant Identifiers: chr20:g.22039898C>A (hg19) ; chr20:g.22059260C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22059260C>A , CM000682.2:g.22059260C>A	GRCh38
NC_000020.10:g.22039898C>A , CM000682.1:g.22039898C>A	GRCh37
NC_000020.9:g.21987898C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_038394.1:n.195+4976C>A