Canonical Allele Identifier: CA1016142121

Gene: LINC01432

Linked Data

• dbSNP Id: rs1982729468
• gnomAD v3: 20-22070089-C-A
• gnomAD v4: 20-22070089-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22070089C>A , CM000682.2:g.22070089C>A	GRCh38
NC_000020.10:g.22050727C>A , CM000682.1:g.22050727C>A	GRCh37
NC_000020.9:g.21998727C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038394.1:n.445+1401C>A