ClinGen Allele Registry
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Canonical Allele Identifier:
CA163157098
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr7:g.99784828G>C
GRCh37
chr7:g.99382451G>C
Linked Data - Sequence & Population
gnomAD v2:
7:99382451 G / C
gnomAD v3:
7:99784828 G / C
gnomAD v4:
chr7-99784828-G-C
Joint Max Group AF
0.06685128 (NFE)
Genomes Max Group AF
0.06685128 (NFE)
Linked Data - NCBI & NCI
dbSNP:
11773597
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.99784828G>C , CM000669.2:g.99784828G>C
GRCh38
NC_000007.13:g.99382451G>C , CM000669.1:g.99382451G>C
GRCh37
NC_000007.12:g.99220387G>C
NCBI36
NG_008421.1:g.4358C>G
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