Canonical Allele Identifier: CA3541875
Gene: MIR146A HGNC NCBI

Linked Data

dbSNP Id: rs2910164
ExAC: 5:159912418 C / G
gnomAD v2: 5-159912418-C-G
gnomAD v3: 5-160485411-C-G
gnomAD v4: 5-160485411-C-G
MyVariant Identifiers: chr5:g.159912418C>G (hg19) chr5:g.159912418_159912419delinsGT (hg19) chr5:g.160485411C>G (hg38) chr5:g.160485411_160485412delinsGT (hg38)
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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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