ClinGen Allele Registry
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Canonical Allele Identifier:
CA15495898
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.95325384C>G
GRCh37
chr7:g.94954696C>G
Linked Data - Sequence & Population
gnomAD v2:
7:94954696 C / G
gnomAD v3:
7:95325384 C / G
gnomAD v4:
chr7-95325384-C-G
Joint Max Group AF
0.52601894 (NFE)
Genomes Max Group AF
0.52601894 (NFE)
Linked Data - NCBI & NCI
dbSNP:
854572
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.95325384C>G , CM000669.2:g.95325384C>G
GRCh38
NC_000007.13:g.94954696C>G , CM000669.1:g.94954696C>G
GRCh37
NC_000007.12:g.94792632C>G
NCBI36
NG_008779.1:g.4189G>C
NG_008779.2:g.4323G>C
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