ClinGen Allele Registry
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Canonical Allele Identifier:
CA76726053
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr3:g.67323553A>G
GRCh37
chr3:g.67373977A>G
Linked Data - Sequence & Population
gnomAD v2:
3:67373977 A / G
gnomAD v3:
3:67323553 A / G
gnomAD v4:
chr3-67323553-A-G
Joint Max Group AF
0.26126397 (MID)
Genomes Max Group AF
0.1560364 (EAS)
Linked Data - NCBI & NCI
dbSNP:
977102
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.67323553A>G , CM000665.2:g.67323553A>G
GRCh38
NC_000003.11:g.67373977A>G , CM000665.1:g.67373977A>G
GRCh37
NC_000003.10:g.67456667A>G
NCBI36
NG_052945.1:g.336062T>C
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