Canonical Allele Identifier: CA11831505
Gene:
MyVariant.info:
GRCh38 chr4:g.73740307A>T
GRCh37 chr4:g.74606024A>T
gnomAD v2:
4:74606024 A / T
gnomAD v3:
4:73740307 A / T
gnomAD v4:
chr4-73740307-A-T
Joint Max Group AF 0.59127115 (EAS)
Genomes Max Group AF 0.59127115 (EAS)
ClinVar RCV:
RCV003312795
ClinVar Variation:
2571395
dbSNP:
4073
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73740307A>T , CM000666.2:g.73740307A>T GRCh38
NC_000004.11:g.74606024A>T , CM000666.1:g.74606024A>T GRCh37
NC_000004.10:g.74824888A>T NCBI36
NG_029889.1:g.4802A>T
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