Canonical Allele Identifier: CA1526081668
Gene: LINC02226 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.8439529G= , CM000667.2:g.8439529G= GRCh38
NC_000005.9:g.8439642G= , CM000667.1:g.8439642G= GRCh37
NC_000005.8:g.8492642G= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_039984.1:n.174+12694C=