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Canonical Allele Identifier:
CA16407310
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.1675619C>T
GRCh37
chr11:g.1696849C>T
Linked Data - Sequence & Population
gnomAD v2:
11:1696849 C / T
gnomAD v3:
11:1675619 C / T
gnomAD v4:
chr11-1675619-C-T
Joint Max Group AF
0.78346767 (EAS)
Genomes Max Group AF
0.78346767 (EAS)
Linked Data - NCBI & NCI
dbSNP:
2334499
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.1675619C>T , CM000673.2:g.1675619C>T
GRCh38
NC_000011.9:g.1696849C>T , CM000673.1:g.1696849C>T
GRCh37
NC_000011.8:g.1653425C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'