Canonical Allele Identifier: CA252649069
Gene: LINC00393 HGNC NCBI

Linked Data

dbSNP Id: rs1172869
MyVariant Identifiers: chr13:g.74066910T>G (hg19) chr13:g.73492773T>G (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
XR_942061.1:n.379-35811A>C
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