ClinGen Allele Registry
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Canonical Allele Identifier:
CA16152185
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr3:g.100237712G>C
GRCh37
chr3:g.99956556G>C
Linked Data - Sequence & Population
gnomAD v2:
3:99956556 G / C
gnomAD v3:
3:100237712 G / C
gnomAD v4:
chr3-100237712-G-C
Joint Max Group AF
0.30930983 (NFE)
Genomes Max Group AF
0.30930983 (NFE)
Linked Data - NCBI & NCI
dbSNP:
12486865
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.100237712G>C , CM000665.2:g.100237712G>C
GRCh38
NC_000003.11:g.99956556G>C , CM000665.1:g.99956556G>C
GRCh37
NC_000003.10:g.101439246G>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'