Canonical Allele Identifier: CA1543249031
Gene: LINC02224 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662262T= , CM000667.2:g.44662262T= GRCh38
NC_000005.9:g.44662364T= , CM000667.1:g.44662364T= GRCh37
NC_000005.8:g.44698121T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427699.2:n.92-3705A=
XR_925983.1:n.71-3705A=