Canonical Allele Identifier: CA179760597
Gene: MIR2052HG HGNC NCBI
LINC03071 HGNC NCBI

Linked Data

dbSNP Id: rs373249843

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.74600742A>G , CM000670.2:g.74600742A>G GRCh38
NC_000008.10:g.75512977A>G , CM000670.1:g.75512977A>G GRCh37
NC_000008.9:g.75675532A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033830.1:n.43+834A>G (MIR2052HG)
XR_929054.1:n.459-10365T>C (LINC03071)
XR_929055.1:n.278-10365T>C (LINC03071)
XR_929057.1:n.336-10365T>C (LINC03071)
XR_001745957.1:n.742-10365T>C (LINC03071)
XR_001745958.1:n.561-10365T>C (LINC03071)
XR_001745960.1:n.336-10365T>C (LINC03071)