Canonical Allele Identifier: CA7350093
Gene: MIR323B HGNC NCBI
gnomAD v2:
14:101522556 T / C
gnomAD v3:
14:101056219 T / C
gnomAD v4:
chr14-101056219-T-C
Joint Max Group AF 0.68034214 (EAS)
Genomes Max Group AF 0.66503059 (EAS)
Exomes Max Group AF 0.68108672 (EAS)
dbSNP:
56103835
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.101056219T>C , CM000676.2:g.101056219T>C GRCh38
NC_000014.8:g.101522556T>C , CM000676.1:g.101522556T>C GRCh37
NC_000014.7:g.100592309T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_036133.1:n.1T>C
Search 100 bp 5'
Search 100 bp 3'