Canonical Allele Identifier: CA9637637
Gene: MIR521-2 HGNC NCBI
MyVariant.info:
GRCh38 chr19:g.53716600G>T
GRCh37 chr19:g.54219854G>T
gnomAD v2:
19:54219854 G / T
gnomAD v3:
19:53716600 G / T
gnomAD v4:
chr19-53716600-G-T
Joint Max Group AF 0.0144484 (AFR)
Genomes Max Group AF 0.01467542 (AFR)
Exomes Max Group AF 0.01213918 (AFR)
dbSNP:
13382089
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53716600G>T , CM000681.2:g.53716600G>T GRCh38
NC_000019.9:g.54219854G>T , CM000681.1:g.54219854G>T GRCh37
NC_000019.8:g.58911666G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_030203.1:n.7G>T
Search 100 bp 5'
Search 100 bp 3'