Canonical Allele Identifier: CA13931721
Gene:
ClinVar RCV:
RCV001724932
ClinVar Variation:
1297228
dbSNP:
1003349
gnomAD v2:
14:23305663 G / T
gnomAD v3:
14:22836454 G / T
gnomAD v4:
chr14-22836454-G-T
Joint Max Group AF 0.39600325 (AMR)
Genomes Max Group AF 0.40706811 (EAS)
Exomes Max Group AF 0.31247816 (EAS)
MyVariant.info:
GRCh38 chr14:g.22836454G>T
GRCh37 chr14:g.23305663G>T
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.22836454G>T , CM000676.2:g.22836454G>T GRCh38
NC_000014.8:g.23305663G>T , CM000676.1:g.23305663G>T GRCh37
NC_000014.7:g.22375503G>T NCBI36
NG_046989.1:g.4922G>T
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