ClinGen Allele Registry
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Canonical Allele Identifier:
CA10849258
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.161502368A>G
GRCh37
chr1:g.161472158A>G
Linked Data - Sequence & Population
gnomAD v2:
1:161472158 A / G
gnomAD v3:
1:161502368 A / G
gnomAD v4:
chr1-161502368-A-G
Joint Max Group AF
0.72929084 (AFR)
Genomes Max Group AF
0.72929084 (AFR)
Linked Data - NCBI & NCI
dbSNP:
10800309
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.161502368A>G , CM000663.2:g.161502368A>G
GRCh38
NC_000001.10:g.161472158A>G , CM000663.1:g.161472158A>G
GRCh37
NC_000001.9:g.159738782A>G
NCBI36
NG_012066.1:g.1954A>G
NG_012066.2:g.1954A>G
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