Canonical Allele Identifier: CA2596083899

Gene: LINC00393

Linked Data

• dbSNP Id: rs2137262774
• gnomAD v3: 13-73492819-G-A
• gnomAD v4: 13-73492819-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.73492819G>A , CM000675.2:g.73492819G>A	GRCh38
NC_000013.10:g.74066956G>A , CM000675.1:g.74066956G>A	GRCh37
NC_000013.9:g.72964957G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_942061.1:n.379-35857C>T