Canonical Allele Identifier: CA1016142443

Gene: LINC01432

Linked Data

• dbSNP Id: rs1982731300
• gnomAD v3: 20-22070135-TG-T
• gnomAD v4: 20-22070135-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22070136del , CM000682.2:g.22070136del	GRCh38
NC_000020.10:g.22050774del , CM000682.1:g.22050774del	GRCh37
NC_000020.9:g.21998774del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038394.1:n.445+1448del