Canonical Allele Identifier: CA610748130

Gene: LINC00393

Linked Data

• dbSNP Id: rs1371423675
• gnomAD v2: 13-74066904-AT-A
• gnomAD v3: 13-73492767-AT-A
• gnomAD v4: 13-73492767-AT-A
• MyVariant Identifiers: chr13:g.74066905del (hg19) ; chr13:g.73492768del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.73492773del , CM000675.2:g.73492773del	GRCh38
NC_000013.10:g.74066910del , CM000675.1:g.74066910del	GRCh37
NC_000013.9:g.72964911del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_942061.1:n.379-35806del