Canonical Allele Identifier: CA652428800
Gene: MIR2052HG HGNC NCBI
LINC03071 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.74615341C>T , CM000670.2:g.74615341C>T GRCh38
NC_000008.10:g.75527576C>T , CM000670.1:g.75527576C>T GRCh37
NC_000008.9:g.75690131C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_033830.1:n.131+2401C>T (MIR2052HG)
XR_929054.1:n.345+1419G>A (LINC03071)
XR_929055.1:n.165-2775G>A (LINC03071)
XR_929056.1:n.345+1419G>A (LINC03071)
XR_929057.1:n.222+1419G>A (LINC03071)
XR_001745957.1:n.628+1419G>A (LINC03071)
XR_001745958.1:n.448-2775G>A (LINC03071)
XR_001745960.1:n.222+1419G>A (LINC03071)
XR_002956714.1:n.628+1419G>A (LINC03071)