Canonical Allele Identifier: CA1115373014
Gene: MIR2052HG HGNC NCBI
LINC03071 HGNC NCBI

Linked Data

dbSNP Id: rs1808265948
gnomAD v3: 8-74615441-T-C
gnomAD v4: 8-74615441-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.74615441T>C , CM000670.2:g.74615441T>C GRCh38
NC_000008.10:g.75527676T>C , CM000670.1:g.75527676T>C GRCh37
NC_000008.9:g.75690231T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033830.1:n.131+2501T>C (MIR2052HG)
XR_929054.1:n.345+1319A>G (LINC03071)
XR_929055.1:n.165-2875A>G (LINC03071)
XR_929056.1:n.345+1319A>G (LINC03071)
XR_929057.1:n.222+1319A>G (LINC03071)
XR_001745957.1:n.628+1319A>G (LINC03071)
XR_001745958.1:n.448-2875A>G (LINC03071)
XR_001745960.1:n.222+1319A>G (LINC03071)
XR_002956714.1:n.628+1319A>G (LINC03071)
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