Canonical Allele Identifier: CA1543249003
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs1739806339

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662227G>A , CM000667.2:g.44662227G>A GRCh38
NC_000005.9:g.44662329G>A , CM000667.1:g.44662329G>A GRCh37
NC_000005.8:g.44698086G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427699.2:n.92-3670C>T
XR_925983.1:n.71-3670C>T