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Canonical Allele Identifier:
CA11047642
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.227850659C>T
GRCh37
chr2:g.228715375C>T
Linked Data - Sequence & Population
gnomAD v2:
2:228715375 C / T
gnomAD v3:
2:227850659 C / T
gnomAD v4:
chr2-227850659-C-T
Joint Max Group AF
0.75847985 (NFE)
Genomes Max Group AF
0.75847985 (NFE)
Linked Data - NCBI & NCI
dbSNP:
7591163
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.227850659C>T , CM000664.2:g.227850659C>T
GRCh38
NC_000002.11:g.228715375C>T , CM000664.1:g.228715375C>T
GRCh37
NC_000002.10:g.228423619C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'