ClinGen Allele Registry
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Canonical Allele Identifier:
CA857454871
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr8:g.98117279G>A
GRCh37
chr8:g.99129507G>A
Linked Data - Sequence & Population
gnomAD v3:
8:98117279 G / A
gnomAD v4:
chr8-98117279-G-A
Joint Max Group AF
0.00000224 (NFE)
Exomes Max Group AF
0.00000115 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2071598
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.98117279G>A , CM000670.2:g.98117279G>A
GRCh38
NC_000008.10:g.99129507G>A , CM000670.1:g.99129507G>A
GRCh37
NC_000008.9:g.99198683G>A
NCBI36
NG_052869.1:g.4987G>A
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