Allele Registry

Canonical Allele Identifier: CA4481364

Gene: MIR96 HGNC NCBI

Linked Data - Predicted Effect Evidence

MyVariant.info:

GRCh38 chr7:g.129774713A>G

GRCh37 chr7:g.129414553A>G

Linked Data - Sequence & Population

gnomAD v2:

7:129414553 A / G

gnomAD v3:

7:129774713 A / G

gnomAD v4:

chr7-129774713-A-G

Joint Max Group AF 0.00014344 (AMR)

Genomes Max Group AF 0.0003065 (AMR)

Exomes Max Group AF 0.00001206 (AMR)

Linked Data - NCBI & NCI

dbSNP:

546098287

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.129774713A>G , CM000669.2:g.129774713A>G	GRCh38
NC_000007.13:g.129414553A>G , CM000669.1:g.129414553A>G	GRCh37
NC_000007.12:g.129201789A>G	NCBI36
NG_023385.1:g.5302T>C

Transcript Alleles

HGVS	Amino-acid Change
NR_029512.1:n.57T>C

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