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Canonical Allele Identifier:
CA12768577
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr8:g.93176690T>G
GRCh37
chr8:g.94188919T>G
Linked Data - Sequence & Population
gnomAD v2:
8:94188919 T / G
gnomAD v3:
8:93176690 T / G
gnomAD v4:
chr8-93176690-T-G
Joint Max Group AF
0.97471038 (EAS)
Genomes Max Group AF
0.97471038 (EAS)
Linked Data - NCBI & NCI
dbSNP:
278600
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.93176690T>G , CM000670.2:g.93176690T>G
GRCh38
NC_000008.10:g.94188919T>G , CM000670.1:g.94188919T>G
GRCh37
NC_000008.9:g.94258095T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'