Canonical Allele Identifier: CA1691423502
Community Standard Title: NC_000007.14:g.17521959A=
Gene: LINC02889 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17521959A= , CM000669.2:g.17521959A= GRCh38
NC_000007.13:g.17561583A= , CM000669.1:g.17561583A= GRCh37
NC_000007.12:g.17528108A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110013.1:n.158+36793T=