ClinGen Allele Registry
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Canonical Allele Identifier:
CA10777662
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr1:g.101414449T>C
GRCh37
chr1:g.101880005T>C
Linked Data - Sequence & Population
gnomAD v2:
1:101880005 T / C
gnomAD v3:
1:101414449 T / C
gnomAD v4:
chr1-101414449-T-C
Joint Max Group AF
0.82124438 (AFR)
Genomes Max Group AF
0.82124438 (AFR)
Linked Data - NCBI & NCI
dbSNP:
2338971
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.101414449T>C , CM000663.2:g.101414449T>C
GRCh38
NC_000001.10:g.101880005T>C , CM000663.1:g.101880005T>C
GRCh37
NC_000001.9:g.101652593T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'