Canonical Allele Identifier: CA1526081685
Gene: LINC02226 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.8439557T= , CM000667.2:g.8439557T= GRCh38
NC_000005.9:g.8439670T= , CM000667.1:g.8439670T= GRCh37
NC_000005.8:g.8492670T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_039984.1:n.174+12666A=