Canonical Allele Identifier: CA1543249067
Gene: LINC02224 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662302A= , CM000667.2:g.44662302A= GRCh38
NC_000005.9:g.44662404A= , CM000667.1:g.44662404A= GRCh37
NC_000005.8:g.44698161A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427699.2:n.92-3745T=
XR_925983.1:n.71-3745T=