Canonical Allele Identifier: CA1526081664
Gene: LINC02226 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.8439521G= , CM000667.2:g.8439521G= GRCh38
NC_000005.9:g.8439634G= , CM000667.1:g.8439634G= GRCh37
NC_000005.8:g.8492634G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_039984.1:n.174+12702C=