Canonical Allele Identifier: CA13934827
Gene:
MyVariant.info:
GRCh38 chr14:g.35405317T>A
GRCh37 chr14:g.35874523T>A
gnomAD v2:
14:35874523 T / A
gnomAD v3:
14:35405317 T / A
gnomAD v4:
chr14-35405317-T-A
Joint Max Group AF 0.16465651 (EAS)
Genomes Max Group AF 0.16465651 (EAS)
ClinVar RCV:
RCV001511879
ClinVar Variation:
1165091
dbSNP:
2233407
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.35405317T>A , CM000676.2:g.35405317T>A GRCh38
NC_000014.8:g.35874523T>A , CM000676.1:g.35874523T>A GRCh37
NC_000014.7:g.34944274T>A NCBI36
NG_007571.1:g.4422A>T , LRG_89:g.4422A>T
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