Canonical Allele Identifier: CA179762229
Gene: MIR2052HG HGNC NCBI
LINC03071 HGNC NCBI
dbSNP:
10106137
gnomAD v2:
8:75527633 C / A
gnomAD v3:
8:74615398 C / A
gnomAD v4:
chr8-74615398-C-A
Joint Max Group AF 0.10755945 (SAS)
Genomes Max Group AF 0.10755945 (SAS)
MyVariant.info:
GRCh38 chr8:g.74615398C>A
GRCh37 chr8:g.75527633C>A
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.74615398C>A , CM000670.2:g.74615398C>A GRCh38
NC_000008.10:g.75527633C>A , CM000670.1:g.75527633C>A GRCh37
NC_000008.9:g.75690188C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033830.1:n.131+2458C>A (MIR2052HG)
XR_929054.1:n.345+1362G>T (LINC03071)
XR_929055.1:n.165-2832G>T (LINC03071)
XR_929056.1:n.345+1362G>T (LINC03071)
XR_929057.1:n.222+1362G>T (LINC03071)
XR_001745957.1:n.628+1362G>T (LINC03071)
XR_001745958.1:n.448-2832G>T (LINC03071)
XR_001745960.1:n.222+1362G>T (LINC03071)
XR_002956714.1:n.628+1362G>T (LINC03071)
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