Canonical Allele Identifier: CA1691423503
Gene: LINC02889 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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