Canonical Allele Identifier: CA2123683117
Gene: LINC00596 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23912266C= , CM000676.2:g.23912266C= GRCh38
NC_000014.8:g.24381475C= , CM000676.1:g.24381475C= GRCh37
NC_000014.7:g.23451315C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_429343.2:n.179-9554G=
XR_001750659.1:n.196-9554G=
XR_429343.3:n.196-9554G=