ClinGen Allele Registry
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Canonical Allele Identifier:
CA10984484
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr1:g.59892297A>G
GRCh37
chr1:g.60357969A>G
Linked Data - Sequence & Population
gnomAD v2:
1:60357969 A / G
gnomAD v3:
1:59892297 A / G
gnomAD v4:
chr1-59892297-A-G
Joint Max Group AF
0.30260275 (SAS)
Genomes Max Group AF
0.30260275 (SAS)
Linked Data - NCBI & NCI
dbSNP:
10789082
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.59892297A>G , CM000663.2:g.59892297A>G
GRCh38
NC_000001.10:g.60357969A>G , CM000663.1:g.60357969A>G
GRCh37
NC_000001.9:g.60130557A>G
NCBI36
NG_007931.1:g.39455T>C
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