ClinGen Allele Registry
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Canonical Allele Identifier:
CA11202056
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.169363371A>G
GRCh37
chr2:g.170219881A>G
Linked Data - Sequence & Population
gnomAD v2:
2:170219881 A / G
gnomAD v3:
2:169363371 A / G
gnomAD v4:
chr2-169363371-A-G
Joint Max Group AF
0.68072038 (AFR)
Genomes Max Group AF
0.68072038 (AFR)
Linked Data - NCBI & NCI
dbSNP:
3755166
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.169363371A>G , CM000664.2:g.169363371A>G
GRCh38
NC_000002.11:g.170219881A>G , CM000664.1:g.170219881A>G
GRCh37
NC_000002.10:g.169928127A>G
NCBI36
NG_012634.1:g.4242T>C
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