Canonical Allele Identifier: CA1543249080
Gene: LINC02224 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662307C= , CM000667.2:g.44662307C= GRCh38
NC_000005.9:g.44662409C= , CM000667.1:g.44662409C= GRCh37
NC_000005.8:g.44698166C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427699.2:n.92-3750G=
XR_925983.1:n.71-3750G=