Canonical Allele Identifier: CA7016174
Gene: MIR17HG HGNC NCBI
MIR92A1 HGNC NCBI
MyVariant.info:
GRCh38 chr13:g.91351335G>A
GRCh37 chr13:g.92003589G>A
gnomAD v2:
13:92003589 G / A
gnomAD v3:
13:91351335 G / A
gnomAD v4:
chr13-91351335-G-A
Joint Max Group AF 0.07042184 (AFR)
Genomes Max Group AF 0.06997256 (AFR)
Exomes Max Group AF 0.06894755 (AFR)
dbSNP:
9589207
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.91351335G>A , CM000675.2:g.91351335G>A GRCh38
NC_000013.10:g.92003589G>A , CM000675.1:g.92003589G>A GRCh37
NC_000013.9:g.90801590G>A NCBI36
NG_032702.1:g.8516G>A

Transcript Alleles

HGVS Amino-acid Change
NR_027349.1:n.284+1109G>A (MIR17HG)
NR_027350.1:n.1778G>A (MIR17HG)
NR_029508.1:n.22G>A (MIR92A1)
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