Canonical Allele Identifier: CA2355184620

Gene: LINC01432

Linked Data

• dbSNP Id: rs1982465884

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22059246G>A , CM000682.2:g.22059246G>A	GRCh38
NC_000020.10:g.22039884G>A , CM000682.1:g.22039884G>A	GRCh37
NC_000020.9:g.21987884G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_038394.1:n.195+4962G>A