Canonical Allele Identifier: CA1543249015
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs1739806492

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662239T>A , CM000667.2:g.44662239T>A GRCh38
NC_000005.9:g.44662341T>A , CM000667.1:g.44662341T>A GRCh37
NC_000005.8:g.44698098T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427699.2:n.92-3682A>T
XR_925983.1:n.71-3682A>T