Canonical Allele Identifier: CA1526081667
Gene: LINC02226 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.8439527G= , CM000667.2:g.8439527G= GRCh38
NC_000005.9:g.8439640G= , CM000667.1:g.8439640G= GRCh37
NC_000005.8:g.8492640G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_039984.1:n.174+12696C=