Canonical Allele Identifier: CA1543248991
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs1312216826

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662210C>A , CM000667.2:g.44662210C>A GRCh38
NC_000005.9:g.44662312C>A , CM000667.1:g.44662312C>A GRCh37
NC_000005.8:g.44698069C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427699.2:n.92-3653G>T
XR_925983.1:n.71-3653G>T