Canonical Allele Identifier: CA2736493201

Gene: LINC01432

Linked Data

• dbSNP Id: rs1982730392

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.22070112_22070113insG , CM000682.2:g.22070112_22070113insG	GRCh38
NC_000020.10:g.22050750_22050751insG , CM000682.1:g.22050750_22050751insG	GRCh37
NC_000020.9:g.21998750_21998751insG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038394.1:n.445+1424_445+1425insG