Canonical Allele Identifier: CA2590604426

Gene: LINC01432

Linked Data

• dbSNP Id: rs2122520788
• gnomAD v3: 20-22070055-C-A
• gnomAD v4: 20-22070055-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22070055C>A , CM000682.2:g.22070055C>A	GRCh38
NC_000020.10:g.22050693C>A , CM000682.1:g.22050693C>A	GRCh37
NC_000020.9:g.21998693C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038394.1:n.445+1367C>A