ClinGen Allele Registry
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Canonical Allele Identifier:
CA177347248
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr8:g.60963416C>G
GRCh37
chr8:g.61875975C>G
Linked Data - Sequence & Population
gnomAD v2:
8:61875975 C / G
gnomAD v3:
8:60963416 C / G
gnomAD v4:
chr8-60963416-C-G
Joint Max Group AF
0.00006802 (NFE)
Genomes Max Group AF
0.00006803 (NFE)
Linked Data - NCBI & NCI
dbSNP:
538835534
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.60963416C>G , CM000670.2:g.60963416C>G
GRCh38
NC_000008.10:g.61875975C>G , CM000670.1:g.61875975C>G
GRCh37
NC_000008.9:g.62038529C>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'