ClinGen Allele Registry
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Canonical Allele Identifier:
CA12678459
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.108670542A>G
GRCh37
chr7:g.108310986A>G
Linked Data - Sequence & Population
gnomAD v2:
7:108310986 A / G
gnomAD v3:
7:108670542 A / G
gnomAD v4:
chr7-108670542-A-G
Joint Max Group AF
0.41140833 (NFE)
Genomes Max Group AF
0.41140833 (NFE)
Linked Data - NCBI & NCI
dbSNP:
193451
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.108670542A>G , CM000669.2:g.108670542A>G
GRCh38
NC_000007.13:g.108310986A>G , CM000669.1:g.108310986A>G
GRCh37
NC_000007.12:g.108098222A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'