ClinGen Allele Registry
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Canonical Allele Identifier:
CA11350217
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.9748794G>A
GRCh37
chr3:g.9790478G>A
Linked Data - Sequence & Population
gnomAD v2:
3:9790478 G / A
gnomAD v3:
3:9748794 G / A
gnomAD v4:
chr3-9748794-G-A
Joint Max Group AF
0.1689485 (NFE)
Genomes Max Group AF
0.1689485 (NFE)
Linked Data - NCBI & NCI
dbSNP:
125701
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.9748794G>A , CM000665.2:g.9748794G>A
GRCh38
NC_000003.11:g.9790478G>A , CM000665.1:g.9790478G>A
GRCh37
NC_000003.10:g.9765478G>A
NCBI36
NG_012106.1:g.3851G>A
NG_052955.1:g.22066G>A
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