Canonical Allele Identifier: CA649991200
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs1739809337

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662496G>A , CM000667.2:g.44662496G>A GRCh38
NC_000005.9:g.44662598G>A , CM000667.1:g.44662598G>A GRCh37
NC_000005.8:g.44698355G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_427699.2:n.92-3939C>T
XR_925983.1:n.71-3939C>T