Canonical Allele Identifier: CA1115380439
Gene: MIR2052HG HGNC NCBI
LINC03071 HGNC NCBI

Linked Data

dbSNP Id: rs1395764706
gnomAD v3: 8-74600817-G-C
gnomAD v4: 8-74600817-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.74600817G>C , CM000670.2:g.74600817G>C GRCh38
NC_000008.10:g.75513052G>C , CM000670.1:g.75513052G>C GRCh37
NC_000008.9:g.75675607G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033830.1:n.43+909G>C (MIR2052HG)
XR_929054.1:n.459-10440C>G (LINC03071)
XR_929055.1:n.278-10440C>G (LINC03071)
XR_929057.1:n.336-10440C>G (LINC03071)
XR_001745957.1:n.742-10440C>G (LINC03071)
XR_001745958.1:n.561-10440C>G (LINC03071)
XR_001745960.1:n.336-10440C>G (LINC03071)