Canonical Allele Identifier: CA957567305

Gene: LINC00393

Linked Data

• dbSNP Id: rs1879180432
• gnomAD v3: 13-73492781-T-C
• gnomAD v4: 13-73492781-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.73492781T>C , CM000675.2:g.73492781T>C	GRCh38
NC_000013.10:g.74066918T>C , CM000675.1:g.74066918T>C	GRCh37
NC_000013.9:g.72964919T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_942061.1:n.379-35819A>G