Canonical Allele Identifier: CA252649071

Gene: LINC00393

Linked Data

• dbSNP Id: rs575746674
• gnomAD v2: 13-74066919-C-A
• gnomAD v3: 13-73492782-C-A
• gnomAD v4: 13-73492782-C-A
• MyVariant Identifiers: chr13:g.74066919C>A (hg19) ; chr13:g.73492782C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.73492782C>A , CM000675.2:g.73492782C>A	GRCh38
NC_000013.10:g.74066919C>A , CM000675.1:g.74066919C>A	GRCh37
NC_000013.9:g.72964920C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_942061.1:n.379-35820G>T