Canonical Allele Identifier: CA1115380451
Gene: MIR2052HG HGNC NCBI
LINC03071 HGNC NCBI

Linked Data

dbSNP Id: rs1004972029
gnomAD v3: 8-74600839-G-T
gnomAD v4: 8-74600839-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.74600839G>T , CM000670.2:g.74600839G>T GRCh38
NC_000008.10:g.75513074G>T , CM000670.1:g.75513074G>T GRCh37
NC_000008.9:g.75675629G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033830.1:n.43+931G>T (MIR2052HG)
XR_929054.1:n.459-10462C>A (LINC03071)
XR_929055.1:n.278-10462C>A (LINC03071)
XR_929057.1:n.336-10462C>A (LINC03071)
XR_001745957.1:n.742-10462C>A (LINC03071)
XR_001745958.1:n.561-10462C>A (LINC03071)
XR_001745960.1:n.336-10462C>A (LINC03071)