Allele Registry

Canonical Allele Identifier: CA176731

Gene: MIR96 HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr7:g.129774734A>G

GRCh37 chr7:g.129414574A>G

Linked Data - Sequence & Population

gnomAD v2:

7:129414574 A / G

gnomAD v3:

7:129774734 A / G

gnomAD v4:

chr7-129774734-A-G

Joint Max Group AF 0.00489619 (NFE)

Genomes Max Group AF 0.00475862 (NFE)

Exomes Max Group AF 0.00482263 (NFE)

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000151023

RCV000992332

ClinVar Variation:

163977

dbSNP:

41274239

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.129774734A>G , CM000669.2:g.129774734A>G	GRCh38
NC_000007.13:g.129414574A>G , CM000669.1:g.129414574A>G	GRCh37
NC_000007.12:g.129201810A>G	NCBI36
NG_023385.1:g.5281T>C

Transcript Alleles

HGVS	Amino-acid Change
NR_029512.1:n.36T>C

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