ClinGen Allele Registry
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Canonical Allele Identifier:
CA10798984
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.7986612C>A
GRCh37
chr1:g.8046672C>A
Linked Data - Sequence & Population
gnomAD v2:
1:8046672 C / A
gnomAD v3:
1:7986612 C / A
gnomAD v4:
chr1-7986612-C-A
Joint Max Group AF
0.16734576 (NFE)
Genomes Max Group AF
0.16734576 (NFE)
Linked Data - NCBI & NCI
dbSNP:
12727642
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.7986612C>A , CM000663.2:g.7986612C>A
GRCh38
NC_000001.10:g.8046672C>A , CM000663.1:g.8046672C>A
GRCh37
NC_000001.9:g.7969259C>A
NCBI36
NG_008271.1:g.29959C>A
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