Canonical Allele Identifier: CA1794225305
Gene: MIR2052HG HGNC NCBI
LINC03071 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.74600829_74600830delinsCT , CM000670.2:g.74600829_74600830delinsCT GRCh38
NC_000008.10:g.75513064_75513065delinsCT , CM000670.1:g.75513064_75513065delinsCT GRCh37
NC_000008.9:g.75675619_75675620delinsCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033830.1:n.43+921_43+922delinsCT (MIR2052HG)
XR_929054.1:n.459-10453_459-10452delinsAG (LINC03071)
XR_929055.1:n.278-10453_278-10452delinsAG (LINC03071)
XR_929057.1:n.336-10453_336-10452delinsAG (LINC03071)
XR_001745957.1:n.742-10453_742-10452delinsAG (LINC03071)
XR_001745958.1:n.561-10453_561-10452delinsAG (LINC03071)
XR_001745960.1:n.336-10453_336-10452delinsAG (LINC03071)