ClinGen Allele Registry
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Canonical Allele Identifier:
CA74607730
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.50314769A>G
GRCh37
chr3:g.50352200A>G
Linked Data - Sequence & Population
gnomAD v2:
3:50352200 A / G
gnomAD v3:
3:50314769 A / G
gnomAD v4:
chr3-50314769-A-G
Joint Max Group AF
0.58103718 (EAS)
Genomes Max Group AF
0.58103718 (EAS)
Linked Data - NCBI & NCI
dbSNP:
11130248
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.50314769A>G , CM000665.2:g.50314769A>G
GRCh38
NC_000003.11:g.50352200A>G , CM000665.1:g.50352200A>G
GRCh37
NC_000003.10:g.50327204A>G
NCBI36
NG_009295.1:g.2613T>C
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