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Canonical Allele Identifier:
CA11001683
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr2:g.15821475G>C
GRCh37
chr2:g.15961599G>C
Linked Data - Sequence & Population
gnomAD v2:
2:15961599 G / C
gnomAD v3:
2:15821475 G / C
gnomAD v4:
chr2-15821475-G-C
Joint Max Group AF
0.82687995 (NFE)
Genomes Max Group AF
0.82687995 (NFE)
Linked Data - NCBI & NCI
dbSNP:
7586898
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.15821475G>C , CM000664.2:g.15821475G>C
GRCh38
NC_000002.11:g.15961599G>C , CM000664.1:g.15961599G>C
GRCh37
NC_000002.10:g.15879050G>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'