ClinGen Allele Registry
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Canonical Allele Identifier:
CA11933638
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr5:g.76714524G>A
GRCh37
chr5:g.76010349G>A
Linked Data - Sequence & Population
gnomAD v2:
5:76010349 G / A
gnomAD v3:
5:76714524 G / A
gnomAD v4:
chr5-76714524-G-A
Joint Max Group AF
0.45357345 (NFE)
Genomes Max Group AF
0.45357345 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2227744
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.76714524G>A , CM000667.2:g.76714524G>A
GRCh38
NC_000005.9:g.76010349G>A , CM000667.1:g.76010349G>A
GRCh37
NC_000005.8:g.76046105G>A
NCBI36
NG_032906.1:g.3482G>A
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