Canonical Allele Identifier: CA252649075

Gene: LINC00393

Linked Data

• dbSNP Id: rs540792912
• MyVariant Identifiers: chr13:g.74066978A>C (hg19) ; chr13:g.73492841A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.73492841A>C , CM000675.2:g.73492841A>C	GRCh38
NC_000013.10:g.74066978A>C , CM000675.1:g.74066978A>C	GRCh37
NC_000013.9:g.72964979A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_942061.1:n.379-35879T>G