Canonical Allele Identifier: CA2766101695
Gene: LINC02224 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662420G>T , CM000667.2:g.44662420G>T GRCh38
NC_000005.9:g.44662522G>T , CM000667.1:g.44662522G>T GRCh37
NC_000005.8:g.44698279G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427699.2:n.92-3863C>A
XR_925983.1:n.71-3863C>A