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Canonical Allele Identifier:
CA10704413
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.228862031C>T
GRCh37
chr1:g.228997778C>T
Linked Data - Sequence & Population
gnomAD v2:
1:228997778 C / T
gnomAD v3:
1:228862031 C / T
gnomAD v4:
chr1-228862031-C-T
Joint Max Group AF
0.01562397 (NFE)
Genomes Max Group AF
0.01562397 (NFE)
Linked Data - NCBI & NCI
dbSNP:
146666914
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.228862031C>T , CM000663.2:g.228862031C>T
GRCh38
NC_000001.10:g.228997778C>T , CM000663.1:g.228997778C>T
GRCh37
NC_000001.9:g.227064401C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'