Canonical Allele Identifier: CA855246544
Gene: MIR2052HG HGNC NCBI
LINC03071 HGNC NCBI

Linked Data

dbSNP Id: rs1421860545
gnomAD v3: 8-74600828-C-G
gnomAD v4: 8-74600828-C-G
MyVariant Identifiers: chr8:g.75513063C>G (hg19) chr8:g.74600828C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.74600828C>G , CM000670.2:g.74600828C>G GRCh38
NC_000008.10:g.75513063C>G , CM000670.1:g.75513063C>G GRCh37
NC_000008.9:g.75675618C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033830.1:n.43+920C>G (MIR2052HG)
XR_929054.1:n.459-10451G>C (LINC03071)
XR_929055.1:n.278-10451G>C (LINC03071)
XR_929057.1:n.336-10451G>C (LINC03071)
XR_001745957.1:n.742-10451G>C (LINC03071)
XR_001745958.1:n.561-10451G>C (LINC03071)
XR_001745960.1:n.336-10451G>C (LINC03071)
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