Allele Registry

Canonical Allele Identifier: CA3541875

Gene: MIR146A HGNC NCBI

Linked Data

dbSNP:

2910164

gnomAD v2:

5:159912418 C / G

gnomAD v3:

5:160485411 C / G

gnomAD v4:

chr5-160485411-C-G

Joint Max Group AF 0.76758767 (NFE)

Genomes Max Group AF 0.76020728 (NFE)

Exomes Max Group AF 0.76881337 (NFE)

MyVariant.info:

GRCh38 chr5:g.160485411C>G

GRCh38 chr5:g.160485411_160485412delinsGT

GRCh37 chr5:g.159912418C>G

GRCh37 chr5:g.159912418_159912419delinsGT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.160485411C>G , CM000667.2:g.160485411C>G	GRCh38
NC_000005.9:g.159912418C>G , CM000667.1:g.159912418C>G	GRCh37
NC_000005.8:g.159844996C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_029701.1:n.60C>G
NR_132748.1:n.303C>G

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