Canonical Allele Identifier: CA610748133

Gene: LINC00393

Linked Data

• dbSNP Id: rs1301144085
• gnomAD v2: 13-74066962-C-T
• gnomAD v3: 13-73492825-C-T
• gnomAD v4: 13-73492825-C-T
• MyVariant Identifiers: chr13:g.74066962C>T (hg19) ; chr13:g.73492825C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.73492825C>T , CM000675.2:g.73492825C>T	GRCh38
NC_000013.10:g.74066962C>T , CM000675.1:g.74066962C>T	GRCh37
NC_000013.9:g.72964963C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_942061.1:n.379-35863G>A