Canonical Allele Identifier: CA1794230461
Gene: MIR2052HG HGNC NCBI
LINC03071 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.74615332A= , CM000670.2:g.74615332A= GRCh38
NC_000008.10:g.75527567A= , CM000670.1:g.75527567A= GRCh37
NC_000008.9:g.75690122A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_033830.1:n.131+2392A= (MIR2052HG)
XR_929054.1:n.345+1428T= (LINC03071)
XR_929055.1:n.165-2766T= (LINC03071)
XR_929056.1:n.345+1428T= (LINC03071)
XR_929057.1:n.222+1428T= (LINC03071)
XR_001745957.1:n.628+1428T= (LINC03071)
XR_001745958.1:n.448-2766T= (LINC03071)
XR_001745960.1:n.222+1428T= (LINC03071)
XR_002956714.1:n.628+1428T= (LINC03071)