Canonical Allele Identifier: CA1016142145

Gene: LINC01432

Linked Data

• dbSNP Id: rs1555784632
• gnomAD v3: 20-22070110-C-CTT
• gnomAD v4: 20-22070110-C-CTT

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22070111_22070112dup , CM000682.2:g.22070111_22070112dup	GRCh38
NC_000020.10:g.22050749_22050750dup , CM000682.1:g.22050749_22050750dup	GRCh37
NC_000020.9:g.21998749_21998750dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038394.1:n.445+1423_445+1424dup