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Canonical Allele Identifier:
CA10689363
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr1:g.162060898C>G
GRCh37
chr1:g.162030688C>G
Linked Data - Sequence & Population
gnomAD v2:
1:162030688 C / G
gnomAD v3:
1:162060898 C / G
gnomAD v4:
chr1-162060898-C-G
Joint Max Group AF
0.62979053 (SAS)
Genomes Max Group AF
0.62979053 (SAS)
Linked Data - NCBI & NCI
dbSNP:
10918594
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.162060898C>G , CM000663.2:g.162060898C>G
GRCh38
NC_000001.10:g.162030688C>G , CM000663.1:g.162030688C>G
GRCh37
NC_000001.9:g.160297312C>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'