Canonical Allele Identifier: CA855246522
Gene: MIR2052HG HGNC NCBI
LINC03071 HGNC NCBI

Linked Data

dbSNP Id: rs1436567071
gnomAD v3: 8-74600814-TC-T
gnomAD v4: 8-74600814-TC-T
MyVariant Identifiers: chr8:g.75513050del (hg19) chr8:g.74600815del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.74600815del , CM000670.2:g.74600815del GRCh38
NC_000008.10:g.75513050del , CM000670.1:g.75513050del GRCh37
NC_000008.9:g.75675605del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033830.1:n.43+907del (MIR2052HG)
XR_929054.1:n.459-10438del (LINC03071)
XR_929055.1:n.278-10438del (LINC03071)
XR_929057.1:n.336-10438del (LINC03071)
XR_001745957.1:n.742-10438del (LINC03071)
XR_001745958.1:n.561-10438del (LINC03071)
XR_001745960.1:n.336-10438del (LINC03071)
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