Canonical Allele Identifier: CA1794225218
Gene: MIR2052HG HGNC NCBI
LINC03071 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.74600749T= , CM000670.2:g.74600749T= GRCh38
NC_000008.10:g.75512984T= , CM000670.1:g.75512984T= GRCh37
NC_000008.9:g.75675539T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033830.1:n.43+841T= (MIR2052HG)
XR_929054.1:n.459-10372A= (LINC03071)
XR_929055.1:n.278-10372A= (LINC03071)
XR_929057.1:n.336-10372A= (LINC03071)
XR_001745957.1:n.742-10372A= (LINC03071)
XR_001745958.1:n.561-10372A= (LINC03071)
XR_001745960.1:n.336-10372A= (LINC03071)