Canonical Allele Identifier: CA2766101686
Gene: LINC02224 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662229T>C , CM000667.2:g.44662229T>C GRCh38
NC_000005.9:g.44662331T>C , CM000667.1:g.44662331T>C GRCh37
NC_000005.8:g.44698088T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427699.2:n.92-3672A>G
XR_925983.1:n.71-3672A>G