Canonical Allele Identifier: CA1794230487
Gene: MIR2052HG HGNC NCBI
LINC03071 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.74615413G= , CM000670.2:g.74615413G= GRCh38
NC_000008.10:g.75527648G= , CM000670.1:g.75527648G= GRCh37
NC_000008.9:g.75690203G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033830.1:n.131+2473G= (MIR2052HG)
XR_929054.1:n.345+1347C= (LINC03071)
XR_929055.1:n.165-2847C= (LINC03071)
XR_929056.1:n.345+1347C= (LINC03071)
XR_929057.1:n.222+1347C= (LINC03071)
XR_001745957.1:n.628+1347C= (LINC03071)
XR_001745958.1:n.448-2847C= (LINC03071)
XR_001745960.1:n.222+1347C= (LINC03071)
XR_002956714.1:n.628+1347C= (LINC03071)