Canonical Allele Identifier: CA179760609
Gene: MIR2052HG HGNC NCBI
LINC03071 HGNC NCBI

Linked Data

dbSNP Id: rs940722441

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.74600811T>C , CM000670.2:g.74600811T>C GRCh38
NC_000008.10:g.75513046T>C , CM000670.1:g.75513046T>C GRCh37
NC_000008.9:g.75675601T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033830.1:n.43+903T>C (MIR2052HG)
XR_929054.1:n.459-10434A>G (LINC03071)
XR_929055.1:n.278-10434A>G (LINC03071)
XR_929057.1:n.336-10434A>G (LINC03071)
XR_001745957.1:n.742-10434A>G (LINC03071)
XR_001745958.1:n.561-10434A>G (LINC03071)
XR_001745960.1:n.336-10434A>G (LINC03071)