Canonical Allele Identifier: CA1899741397
Community Standard Title: NC_000010.11:g.31223169T=
Gene: LINC02664 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.31223169T= , CM000672.2:g.31223169T= GRCh38
NC_000010.10:g.31512098T= , CM000672.1:g.31512098T= GRCh37
NC_000010.9:g.31552104T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_134478.1:n.317+34970T=
XR_242751.2:n.490+34970T=