Canonical Allele Identifier: CA179760612
Gene: MIR2052HG HGNC NCBI
LINC03071 HGNC NCBI

Linked Data

dbSNP Id: rs1027400931
gnomAD v3: 8-74600833-C-G
gnomAD v4: 8-74600833-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.74600833C>G , CM000670.2:g.74600833C>G GRCh38
NC_000008.10:g.75513068C>G , CM000670.1:g.75513068C>G GRCh37
NC_000008.9:g.75675623C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033830.1:n.43+925C>G (MIR2052HG)
XR_929054.1:n.459-10456G>C (LINC03071)
XR_929055.1:n.278-10456G>C (LINC03071)
XR_929057.1:n.336-10456G>C (LINC03071)
XR_001745957.1:n.742-10456G>C (LINC03071)
XR_001745958.1:n.561-10456G>C (LINC03071)
XR_001745960.1:n.336-10456G>C (LINC03071)