ClinGen Allele Registry
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Canonical Allele Identifier:
CA10900156
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.29792805T>C
GRCh37
chr1:g.30265652T>C
Linked Data - Sequence & Population
gnomAD v2:
1:30265652 T / C
gnomAD v3:
1:29792805 T / C
gnomAD v4:
chr1-29792805-T-C
Joint Max Group AF
0.88628452 (NFE)
Genomes Max Group AF
0.88628452 (NFE)
Linked Data - NCBI & NCI
dbSNP:
6691847
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.29792805T>C , CM000663.2:g.29792805T>C
GRCh38
NC_000001.10:g.30265652T>C , CM000663.1:g.30265652T>C
GRCh37
NC_000001.9:g.30038239T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'