Canonical Allele Identifier: CA252649072

Gene: LINC00393

Linked Data

• dbSNP Id: rs993307270
• MyVariant Identifiers: chr13:g.74066933G>A (hg19) ; chr13:g.73492796G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.73492796G>A , CM000675.2:g.73492796G>A	GRCh38
NC_000013.10:g.74066933G>A , CM000675.1:g.74066933G>A	GRCh37
NC_000013.9:g.72964934G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_942061.1:n.379-35834C>T