Canonical Allele Identifier: CA2101852542
Gene: LINC00393 HGNC NCBI

Linked Data

dbSNP Id: rs1879180729

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.73492783C>T , CM000675.2:g.73492783C>T GRCh38
NC_000013.10:g.74066920C>T , CM000675.1:g.74066920C>T GRCh37
NC_000013.9:g.72964921C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_942061.1:n.379-35821G>A