Canonical Allele Identifier: CA13956595
Gene:
MyVariant.info:
GRCh38 chr14:g.35405593G>A
GRCh37 chr14:g.35874799G>A
gnomAD v2:
14:35874799 G / A
gnomAD v3:
14:35405593 G / A
gnomAD v4:
chr14-35405593-G-A
Joint Max Group AF 0.28641652 (NFE)
Genomes Max Group AF 0.28641652 (NFE)
ClinVar RCV:
RCV001517840
ClinVar Variation:
1167989
dbSNP:
2233406
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.35405593G>A , CM000676.2:g.35405593G>A GRCh38
NC_000014.8:g.35874799G>A , CM000676.1:g.35874799G>A GRCh37
NC_000014.7:g.34944550G>A NCBI36
NG_007571.1:g.4146C>T , LRG_89:g.4146C>T
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