Canonical Allele Identifier: CA1794225313
Gene: MIR2052HG HGNC NCBI
LINC03071 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.74600835A= , CM000670.2:g.74600835A= GRCh38
NC_000008.10:g.75513070A= , CM000670.1:g.75513070A= GRCh37
NC_000008.9:g.75675625A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033830.1:n.43+927A= (MIR2052HG)
XR_929054.1:n.459-10458T= (LINC03071)
XR_929055.1:n.278-10458T= (LINC03071)
XR_929057.1:n.336-10458T= (LINC03071)
XR_001745957.1:n.742-10458T= (LINC03071)
XR_001745958.1:n.561-10458T= (LINC03071)
XR_001745960.1:n.336-10458T= (LINC03071)