Canonical Allele Identifier: CA2503781969
Gene: LINC02224 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662266C>A , CM000667.2:g.44662266C>A GRCh38
NC_000005.9:g.44662368C>A , CM000667.1:g.44662368C>A GRCh37
NC_000005.8:g.44698125C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427699.2:n.92-3709G>T
XR_925983.1:n.71-3709G>T