Canonical Allele Identifier: CA1543249089
Gene: LINC02224 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662321T= , CM000667.2:g.44662321T= GRCh38
NC_000005.9:g.44662423T= , CM000667.1:g.44662423T= GRCh37
NC_000005.8:g.44698180T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427699.2:n.92-3764A=
XR_925983.1:n.71-3764A=